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: rs141723617
rs141723617
1 1.000 0.040 7 117530999 missense variant T/C snv 7.1E-04 2.7E-04 0.010 1.000 1 2006 2006
dbSNP: rs1800076
rs1800076
10 0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 0.010 1.000 1 2014 2014