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: rs17174794
rs17174794
1 1.000 6 154089975 missense variant C/G;T snv 4.1E-03 0.010 1.000 1 2013 2013
dbSNP: rs17174801
rs17174801
1 1.000 6 154089989 missense variant A/G snv 6.9E-04 2.8E-03 0.010 1.000 1 2013 2013
dbSNP: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2013 2013
dbSNP: rs62638690
rs62638690
2 0.925 0.080 6 154090110 missense variant G/T snv 5.6E-03 5.6E-03 0.010 1.000 1 2013 2013