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: rs137853903
rs137853903
1 1.000 0.080 6 42188686 missense variant C/T snv 1.3E-03 5.1E-03 0.010 1.000 1 2004 2004
dbSNP: rs531673296
rs531673296
1 1.000 0.080 6 42185706 missense variant A/C snv 9.9E-05 2.8E-04 0.010 1.000 1 2004 2004