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: rs864745
rs864745
12 0.763 0.320 7 28140937 intron variant T/C snv 0.41 0.890 0.929 14 2008 2017
dbSNP: rs849134
rs849134
1 1.000 0.080 7 28156603 intron variant A/G snv 0.41 0.800 1.000 3 2010 2016
dbSNP: rs849135
rs849135
2 0.925 0.120 7 28156794 intron variant G/A snv 0.40 0.800 1.000 3 2012 2018
dbSNP: rs1635852
rs1635852
5 0.882 0.160 7 28149792 intron variant T/C snv 0.42 0.710 1.000 2 2013 2019
dbSNP: rs1708302
rs1708302
1 1.000 0.080 7 28159058 intron variant C/T snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs860262
rs860262
6 0.807 0.200 7 28154778 intron variant C/A;T snv 0.41 0.700 1.000 1 2019 2019
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