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 0.800 0.895 19 2004 2017
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.100 0.929 14 2005 2018
dbSNP: rs1191926239
rs1191926239
7 0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs12377632
rs12377632
5 0.827 0.120 9 117710452 intron variant T/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs1554973
rs1554973
3 0.882 0.120 9 117718534 3 prime UTR variant T/C snv 0.38 0.010 1.000 1 2014 2014
dbSNP: rs754342091
rs754342091
7 0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 0.010 1.000 1 2015 2015