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: rs4986790
rs4986790
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.060 1.000 6 2004 2019
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2015
dbSNP: rs10759932
rs10759932
15 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs1371329921
rs1371329921
2 0.925 0.080 9 117712993 stop gained C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2010 2010
dbSNP: rs1927906
rs1927906
1 1.000 0.080 9 117717837 3 prime UTR variant T/C snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs7873784
rs7873784
11 0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2015 2015