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: rs1208512558
rs1208512558
2 0.925 0.040 2 25161623 missense variant C/G;T snv 6.7E-06 0.010 1.000 1 2002 2002
dbSNP: rs1449052677
rs1449052677
3 0.882 0.120 2 25161643 missense variant T/C snv 1.3E-05 0.010 1.000 1 2002 2002