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: rs1344706
rs1344706
21 0.701 0.160 2 184913701 intron variant A/C;T snv 0.900 0.873 63 2008 2019
dbSNP: rs7597593
rs7597593
6 0.827 0.160 2 184668853 intron variant T/C snv 0.53 0.720 1.000 5 2011 2019
dbSNP: rs11693094
rs11693094
1 1.000 0.040 2 184736693 intron variant C/T snv 0.38 0.700 1.000 4 2014 2019
dbSNP: rs10196799
rs10196799
1 1.000 0.040 2 184776001 intron variant A/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs4666990
rs4666990
2 1.000 0.040 2 184798577 intron variant T/C snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs62200787
rs62200787
1 1.000 0.040 2 184862626 intron variant T/A snv 9.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs62200793
rs62200793
2 0.925 0.040 2 184885915 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs12476147
rs12476147
4 0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 0.020 1.000 2 2014 2018
dbSNP: rs1366842
rs1366842
1 1.000 0.040 2 184937516 missense variant C/A;T snv 0.59; 4.1E-06 0.020 1.000 2 2012 2016
dbSNP: rs13423388
rs13423388
1 1.000 0.040 2 184915498 intron variant G/A snv 0.15 0.010 1.000 1 2011 2011
dbSNP: rs359895
rs359895
1 1.000 0.040 2 184598458 non coding transcript exon variant T/A snv 0.57 0.010 1.000 1 2011 2011
dbSNP: rs3731834
rs3731834
1 1.000 0.040 2 184938637 missense variant C/G snv 0.17 0.14 0.010 1.000 1 2012 2012
dbSNP: rs56280129
rs56280129
1 1.000 0.040 2 184915579 intron variant G/A snv 5.8E-04 0.010 1.000 1 2011 2011
dbSNP: rs61739290
rs61739290
1 1.000 0.040 2 184936870 missense variant A/G snv 5.4E-02 5.4E-02 0.010 1.000 1 2012 2012