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: rs104893967
rs104893967
5 0.827 0.080 6 42178374 missense variant A/G snv 0.700 1.000 1 1998 1998
dbSNP: rs771261841
rs771261841
1 1.000 0.080 6 42178419 missense variant C/T snv 3.6E-05 7.0E-05 0.010 1.000 1 2004 2004