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: rs80358284
rs80358284
10 0.790 0.240 11 86952443 missense variant T/A;C snv 4.0E-06; 2.4E-05 0.700 0
dbSNP: rs774200714
rs774200714
1 1.000 0.160 11 86954909 missense variant G/T snv 3.6E-05 5.6E-05 0.010 1.000 1 1997 1997