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: rs1060502607
rs1060502607
1 1.000 0.120 19 46608846 missense variant G/C snv 0.700 1.000 5 2013 2016
dbSNP: rs1060502608
rs1060502608
1 1.000 0.120 19 46608584 missense variant A/C snv 0.700 0
dbSNP: rs1555814427
rs1555814427
1 1.000 0.120 19 46609125 missense variant A/G snv 0.700 0