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: rs1223231582
rs1223231582
24 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 0.020 1.000 2 2002 2006
dbSNP: rs768051473
rs768051473
1 1.000 0.080 7 142750587 missense variant G/A;C snv 2.4E-05; 8.0E-06 0.010 1.000 1 2006 2006