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: rs12722502
rs12722502
4 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 0.700 1.000 2 2019 2019
dbSNP: rs61839660
rs61839660
9 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs9663421
rs9663421
1 1.000 0.080 10 6013641 intron variant C/A;T snv 0.700 1.000 1 2019 2019