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: rs849142
rs849142
6 0.807 0.240 7 28146272 intron variant T/C snv 0.39 0.700 1.000 2 2009 2015
dbSNP: rs10245867
rs10245867
2 0.925 0.080 7 28102567 intron variant G/T snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs12531540
rs12531540
1 1.000 0.080 7 28123055 intron variant C/T snv 0.36 0.700 1.000 1 2015 2015
dbSNP: rs1635852
rs1635852
5 0.882 0.160 7 28149792 intron variant T/C snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs702814
rs702814
2 1.000 0.080 7 28133113 intron variant C/T snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs849136
rs849136
4 0.851 0.240 7 28135338 intron variant A/G snv 0.74 0.010 < 0.001 1 2010 2010
dbSNP: rs849140
rs849140
7 0.851 0.240 7 28144083 intron variant T/C snv 0.58 0.010 < 0.001 1 2010 2010
dbSNP: rs849141
rs849141
6 0.851 0.240 7 28145472 intron variant A/G snv 0.78 0.010 < 0.001 1 2010 2010
dbSNP: rs864745
rs864745
12 0.763 0.320 7 28140937 intron variant T/C snv 0.41 0.010 < 0.001 1 2010 2010