Source: BEFREE ×
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: rs1059702
rs1059702
7 0.807 0.280 X 154018741 missense variant A/G snv 0.72 0.010 1.000 1 2015 2015
dbSNP: rs1370128
rs1370128
2 0.925 0.160 12 66224858 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs1624395
rs1624395
2 0.925 0.160 12 66224436 intron variant A/G snv 0.63 0.010 1.000 1 2015 2015