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: rs80338831
rs80338831
4 0.882 0.320 22 36292060 missense variant C/A;G;T snv 0.020 1.000 2 2003 2003
dbSNP: rs80338826
rs80338826
6 0.827 0.320 22 36305985 missense variant G/A snv 0.010 1.000 1 2002 2002