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
8 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 0.967 7 2007 2017
dbSNP: rs3821236
rs3821236
3 0.882 0.160 2 191038032 intron variant G/A snv 0.25 0.810 1.000 2 2008 2016
dbSNP: rs7601754
rs7601754
2 0.882 0.160 2 191075725 intron variant G/A;T snv 0.810 1.000 1 2010 2013
dbSNP: rs10168266
rs10168266
3 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs10931481
rs10931481
2 0.827 0.240 2 191090126 intron variant G/A snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs1517352
rs1517352
3 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: rs7594501
rs7594501
1 1.000 0.080 2 191073874 intron variant G/A snv 8.7E-02 0.700 1.000 1 2013 2013