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: rs7574865
rs7574865
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.967 30 2007 2017
dbSNP: rs3821236
rs3821236
3 0.882 0.160 2 191038032 intron variant G/A snv 0.25 0.810 1.000 3 2008 2016
dbSNP: rs7601754
rs7601754
3 0.882 0.160 2 191075725 intron variant G/A;T snv 0.810 1.000 3 2010 2013
dbSNP: rs7582694
rs7582694
9 0.763 0.400 2 191105394 intron variant C/G snv 0.77 0.740 1.000 6 2008 2017
dbSNP: rs11889341
rs11889341
12 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.710 1.000 5 2015 2018
dbSNP: rs10168266
rs10168266
8 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs10174238
rs10174238
14 0.724 0.200 2 191108308 intron variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs10931481
rs10931481
5 0.827 0.240 2 191090126 intron variant G/A snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs12612769
rs12612769
1 1.000 0.080 2 191089272 intron variant A/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs13389408
rs13389408
4 0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs1517352
rs1517352
5 0.851 0.160 2 191066738 intron variant A/C snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs16833239
rs16833239
1 1.000 0.080 2 191075534 intron variant G/A snv 8.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs6736175
rs6736175
1 1.000 0.080 2 191081596 intron variant C/T snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs7568275
rs7568275
6 0.827 0.120 2 191101726 intron variant G/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7594501
rs7594501
1 1.000 0.080 2 191073874 intron variant G/A snv 8.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs10181656
rs10181656
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.020 1.000 2 2008 2010
dbSNP: rs16833215
rs16833215
1 1.000 0.080 2 191049073 intron variant A/G snv 0.34 0.010 1.000 1 2013 2013