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: rs11552822
rs11552822
2 1.000 9 21971109 missense variant C/A;T snv 4.3E-06 0.700 0
dbSNP: rs747621669
rs747621669
1 9 21970988 missense variant C/T snv 4.1E-06 0.700 0