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: rs1197981811
rs1197981811
1 1.000 0.120 6 52025059 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.700 1.000 10 2002 2015