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: rs1264858438
rs1264858438
2 0.925 0.080 20 63406931 missense variant C/T snv 9.0E-06 1.4E-05 0.010 1.000 1 2008 2008
dbSNP: rs201868078
rs201868078
2 0.925 0.040 20 63408524 missense variant G/A;C snv 1.6E-05 0.010 1.000 1 2008 2008