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: rs11575934
rs11575934
4 0.882 0.040 19 18075808 missense variant T/C snv 0.28 0.25 0.010 1.000 1 2007 2007
dbSNP: rs11575935
rs11575935
2 0.925 0.040 19 18063921 missense variant C/T snv 1.1E-02 5.7E-03 0.010 1.000 1 2007 2007
dbSNP: rs375947
rs375947
2 1.000 0.040 19 18069641 missense variant A/G snv 0.29 0.29 0.010 1.000 1 2007 2007
dbSNP: rs401502
rs401502
2 0.925 0.040 19 18069603 missense variant C/A;G;T snv 0.28; 3.2E-05 0.010 1.000 1 2007 2007