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: rs11076962
rs11076962
2 16 5761366 intron variant T/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs11077204
rs11077204
1 16 7617185 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11077207
rs11077207
1 16 7618478 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11646221
rs11646221
1 16 7616086 intron variant G/T snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs11865256
rs11865256
1 16 7215069 intron variant C/T snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs12709186
rs12709186
1 16 7199471 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs3785238
rs3785238
1 16 7615555 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7186834
rs7186834
1 16 7623253 intron variant T/C snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs9934041
rs9934041
1 16 7179578 intron variant C/T snv 0.32 0.700 1.000 1 2018 2018