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: rs1460260991
rs1460260991
1 1.000 0.040 3 52203996 synonymous variant A/G snv 4.1E-06 0.010 1.000 1 1998 1998
dbSNP: rs200361165
rs200361165
1 1.000 0.040 3 52212412 missense variant A/C;G snv 1.2E-05 0.010 1.000 1 1999 1999