Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7466269
rs7466269
2 9 130588697 intron variant A/G snv 0.33 0.700 1.000 5 2008 2017
dbSNP: rs10901216
rs10901216
2 9 130596504 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11792294
rs11792294
1 9 130606619 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018