
Datasets and Cohorts
GWAS dataset |
Cases |
Controls |
Reference |
NatGen 2016 Any migraine |
59 674 | 316 078 | |
NatGen 2016 MA only |
6 332 | 144 883 | |
NatGen 2016 MO only |
8 348 | 139 622 | |
NatGen 2013 Any migraine |
23 285 |
95 425 |
|
NatGen 2012 Clinical MO |
2 326 | 4 580 | |
NatGen 2010 Clinical MA |
2 731 | 10 747 |
Cohorts (Population-based)
ALSPAC (The Avon Longitudinal Study of Parents and Children)
B58C (British 1958 Birth Cohort)
ERF (The Erasmus Rucphen Family Study)
FinnTwin (Finnish Twin Cohort)
HUNT (The Nord-Trøndelag Health Study)
NTR (the Netherlands Twin Registry)
NESDA (the Netherlands Study of Depression and Anxiety)
NFBC (Northern Finland Birth Cohort)
The Women’s Genome Health Study (WGHS)
Hautakangas et al. Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. 2021 medRxiv https://doi.org/10.1101/2021.01.20.21249647
Summary statistics with P < 5e-8
File of 8,117 SNPs (migraine_ihgc2021_gws_gwama.txt and README_migraine_ihgc2021_gws_gwama).
Genome-wide summary statistics for the four other study collections except 23andMe are available for bona fide researchers (contact Dr. Dale Nyholt, d.nyholt@qut.edu.au, for the link to data). The full GWAS summary statistics for the 23andMe discovery data set will be made available through 23andMe to qualified researchers under an agreement with 23andMe that protects the privacy of the 23andMe participants. Please visit research.23andme.com/collaborate/#publication for more information and to apply to access the data.
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