---
title: "NG00058 – Summary Statistics of IGAP Age at onset survival GWAS dataset – Huang et al., 2017"
id: "9251"
type: "dataset"
slug: "ng00058"
published_at: "2026-08-20T14:25:43+00:00"
modified_at: "2026-08-25T19:13:58+00:00"
url: "https://dss.niagads.org/datasets/ng00058/"
markdown_url: "https://dss.niagads.org/datasets/ng00058.md"
excerpt: "To access the full dataset, please log into DSS and submit an application.Within the application, add this dataset (accession NG00058) in the “Choose a Dataset” section.Once approved, you will be able to log in and access the data within the..."
taxonomy_dataset_categories:
  - "AD"
  - "Controlled Access"
  - "Data Type"
  - "Disease"
  - "Open Access"
  - "Open and Controlled Access Data"
  - "Summary Statistics"
---

## Overview

To access the full dataset, please log into DSS and submit an application.  
Within the application, add this dataset (accession NG00058) in the “Choose a Dataset” section.  
Once approved, you will be able to log in and access the data within the DARM portal.

The p-value only files are available in the “Open Access Dataset” tab.

This dataset was originally published on the NIAGADS archive site and was moved to DSS on 08/28/2026.

#### Description

The genome-wide survival association study was performed on 14,406 AD case samples and 25,849 control samples from the International Genomics of Alzheimer’s Project (IGAP) consortium (see Table 1a, [Huang et al., 2017](https://www.ncbi.nlm.nih.gov/pubmed/28628103)
 for details). The final IGAP meta-analysis dataset consists of samples from the Alzheimer’s Disease Genetics Consortium (ADGC), Genetic and Environmental Risk in Alzheimer’s Disease (GERAD), European Alzheimer’s Disease Initiative (EADI), and Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE). The study cohorts consist of case–control and longitudinal cohorts and are described in detail in online methods of ([Huang et al., 2017](https://www.ncbi.nlm.nih.gov/pubmed/28628103)
). 8,253,925 imputed and genotyped SNPs passed quality control and were included for meta-analysis across all cohorts. There was no evidence of genomic inflation (λ = 1.026).

Four loci showed genome-wide significant associations with AAOS: BIN1 (P = 3.9×10−10), MS4A (P = 2.3×10−9), PICALM (P = 9.1×10−12) and APOE (P = 7.8×10−52)). Four other AD risk loci previously reported in the IGAP GWAS showed associations that reached suggestive significance: CR1 (P = 1.2×10−6), SPI1 (previously labeled as CELF1 in the 2013 IGAP GWAS paper1; P = 8.4×10−6), SORL1 (P = 5.5×10−6) and FERMT2 (P = 2.3×10−6). We also identified 14 loci that reached suggestive significance in the survival analysis, three of which (rs116341973, rs1625716 and rs11074412) were nominally associated with AD risk.

#### Available Filesets

| Name | Accession | Latest Release | Description |
| --- | --- | --- | --- |
| IGAP Age at Onset Survival: Full Summary Statistics (application needed) | fsa000177 | NG00058.v1 | Full Summary Statistics |
| IGAP Age at Onset Survival: P-value Only (open access) | fsa000178 | NG00058.v1 | P-value Only |

View the [File Manifest](https://st1.niagads.org/portal/download-public/NG00058.v1/fm)
 for a full list of files released in this dataset.

## Related Studies

- [sa000086 - Summary Statistics of IGAP Age at onset survival GWAS dataset - Huang et al., 2017](https://dss.niagads.org/studies/sa000086/) A genome-wide survival analysis of 14,406 Alzheimer's disease (AD) cases and 25,849 controls identified eight previously reported AD risk loci and 14 novel loci associated with age at onset. Linkage… [Learn more](https://dss.niagads.org/studies/sa000086/)

## Acknowledgement

### Acknowledgment statement for any data distributed by NIAGADS:

Data for this study were prepared, archived, and distributed by the National Institute on Aging Alzheimer's Disease Data Storage Site (NIAGADS) at the University of Pennsylvania (U24-AG041689), funded by the National Institute on Aging.

Use the study-specific acknowledgement statements below (as applicable):

### For investigators using any data from this dataset:

Please cite/reference the use of NIAGADS data by including the accession [NG00058](https://archive.niagads.org/datasets/NG00058)
.

### For investigators using Summary Statistics of IGAP Age at onset survival GWAS dataset – Huang et al., 2017 (sa000086) data:

This work was supported by grants from the National Institutes of Health (U01AG049508, R01-AG035083 and RF-AG054011 (to A.M.G.) and R01-AG044546 and RF1AG053303 (to C.C.)), the JPB Foundation (to A.M.G.) and F Prime (to A.M.G.). Kuan-lin Huang received fellowship funding in part from the Ministry of Education in Taiwan and the Lucille P. Markey Special Emphasis Pathway in Human Pathobiology. Ke Hao is partially supported by the National Natural Science Foundation of China (Grant Nos. 21477087 and 91643201) and by the Ministry of Science and Technology of China (Grant No. 2016YFC0206507). For a detailed list of support for IGAP sample datasets please see Huang et al., 2017)

We thank the [International Genomics of Alzheimer's Project (IGAP)](http://web.pasteur-lille.fr/en/recherche/u744/igap/igap_download.php)
 for providing summary results data for these analyses. The investigators within IGAP contributed to the design and implementation of IGAP and/or provided data but did not participate in analysis or writing of this report. IGAP was made possible by the generous participation of the control subjects, the patients, and their families. The i–Select chips was funded by the French National Foundation on Alzheimer's disease and related disorders. EADI was supported by the LABEX (laboratory of excellence program investment for the future) DISTALZ grant, Inserm, Institut Pasteur de Lille, Université de Lille 2 and the Lille University Hospital. GERAD was supported by the Medical Research Council (Grant n° 503480), Alzheimer's Research UK (Grant n° 503176), the Wellcome Trust (Grant n° 082604/2/07/Z) and German Federal Ministry of Education and Research (BMBF): Competence Network Dementia (CND) grant n° 01GI0102, 01GI0711, 01GI0420. CHARGE was partly supported by the NIH/NIA grant R01 AG033193 and the NIA AG081220 and AGES contract N01–AG–12100, the NHLBI grant R01 HL105756, the Icelandic Heart Association, and the Erasmus Medical Center and Erasmus University. ADGC was supported by the NIH/NIA grants: U01 AG032984, U24 AG021886, U01 AG016976, and the Alzheimer's Association grant ADGC–10–196728.

## Publications

- Lambert JC. **Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.***Nature genetics. 2013 Dec.*[PubMed link](https://pubmed.ncbi.nlm.nih.gov/24162737/)
- Huang KL. **A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease.***Nature neuroscience. 2017 Aug.*[PubMed link](https://pubmed.ncbi.nlm.nih.gov/28628103/)

### Total number of participants: 0