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: rs104894231
rs104894231
9 0.776 0.360 11 533467 missense variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs112445441
rs112445441
32 0.658 0.400 12 25245347 missense variant C/A;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs121913527
rs121913527
9 0.807 0.320 12 25225628 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs773225979
rs773225979
1 1.000 0.120 8 38428364 missense variant T/C snv 2.4E-05 0.010 1.000 1 2019 2019
dbSNP: rs867532966
rs867532966
1 1.000 0.120 8 38413738 missense variant T/C snv 0.010 1.000 1 2019 2019