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: rs1129844
rs1129844
13 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 0.010 1.000 1 2007 2007
dbSNP: rs1411351750
rs1411351750
1 1.000 0.080 17 34285859 synonymous variant C/T snv 4.0E-06 0.010 < 0.001 1 2007 2007