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: rs74315486
rs74315486
1 1.000 22 26625603 missense variant T/C snv 0.800 1.000 2 2006 2010
dbSNP: rs74315487
rs74315487
1 1.000 22 26625528 missense variant T/C snv 0.800 1.000 2 2006 2010
dbSNP: rs1114167427
rs1114167427
1 1.000 22 26625512 missense variant G/T snv 0.700 1.000 2 2006 2010