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: rs1057519739
rs1057519739
2 1.000 0.080 18 51065518 missense variant G/A;C snv 0.700 0
dbSNP: rs1555685186
rs1555685186
1 1.000 0.080 18 51048824 missense variant C/T snv 0.700 0
dbSNP: rs377767347
rs377767347
14 0.742 0.520 18 51065549 missense variant G/A;C;T snv 0.700 0