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: rs754680319
rs754680319
1 1.000 0.120 10 71819769 missense variant C/G snv 1.6E-05 0.010 1.000 1 2003 2003
dbSNP: rs770171865
rs770171865
2 0.925 0.120 10 71828089 missense variant G/T snv 2.4E-05 0.010 1.000 1 1999 1999