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: rs104894845
rs104894845
8 0.807 0.160 X 101401752 missense variant C/G;T snv 5.5E-04 0.010 1.000 1 2018 2018
dbSNP: rs28935197
rs28935197
10 0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 0.010 1.000 1 2012 2012
dbSNP: rs28935485
rs28935485
3 0.925 0.160 X 101398534 missense variant G/C snv 0.010 1.000 1 2012 2012