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: rs203462
rs203462
7 0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 0.010 1.000 1 2007 2007
dbSNP: rs796096871
rs796096871
6 0.807 0.200 17 19909228 missense variant TG/CA mnv 0.010 1.000 1 2007 2007