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: rs372958987
rs372958987
1 1.000 0.080 20 59324430 missense variant C/A;G;T snv 2.0E-05; 3.6E-05 0.010 1.000 1 1998 1998
dbSNP: rs868107957
rs868107957
1 1.000 0.080 20 59301574 missense variant G/A snv 4.0E-06 0.010 1.000 1 2001 2001