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 0.070 0.714 7 2006 2018
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.040 0.500 4 2011 2018
dbSNP: rs10759932
rs10759932
15 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 0.010 1.000 1 2015 2015
dbSNP: rs11536891
rs11536891
4 0.851 0.120 9 117717059 3 prime UTR variant T/C snv 0.16 0.010 1.000 1 2009 2009
dbSNP: rs1420111973
rs1420111973
2 1.000 0.080 9 117712527 synonymous variant T/C snv 7.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs1927911
rs1927911
28 0.658 0.640 9 117707776 intron variant A/G snv 0.62 0.010 1.000 1 2014 2014
dbSNP: rs5030728
rs5030728
7 0.807 0.160 9 117712004 intron variant G/A;T snv 0.23 0.010 1.000 1 2015 2015
dbSNP: rs7873784
rs7873784
11 0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2009 2009