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: rs7756992
rs7756992
9 0.827 0.240 6 20679478 intron variant A/G;T snv 0.900 0.966 21 2007 2019
dbSNP: rs7754840
rs7754840
8 0.807 0.200 6 20661019 intron variant G/A;C;T snv 0.900 0.958 15 2007 2019
dbSNP: rs10946398
rs10946398
5 0.827 0.160 6 20660803 intron variant A/C snv 0.40 0.900 1.000 10 2007 2019
dbSNP: rs4712523
rs4712523
1 0.925 0.120 6 20657333 intron variant A/G snv 0.41 0.830 1.000 3 2009 2019
dbSNP: rs9465871
rs9465871
2 0.882 0.120 6 20717024 intron variant T/C snv 0.30 0.830 1.000 3 2007 2017
dbSNP: rs10440833
rs10440833
1 1.000 0.080 6 20687890 intron variant T/A;G snv 0.26 0.820 1.000 2 2010 2019
dbSNP: rs4712524
rs4712524
1 0.925 0.120 6 20657634 intron variant A/G snv 0.40 0.820 1.000 2 2008 2019
dbSNP: rs6931514
rs6931514
1 0.925 0.120 6 20703721 intron variant A/G snv 0.27 0.820 1.000 2 2007 2012
dbSNP: rs35612982
rs35612982
1 1.000 0.080 6 20682391 intron variant T/C snv 0.29 0.710 1.000 1 2016 2019
dbSNP: rs11757677
rs11757677
1 1.000 0.080 6 21072798 intron variant G/A snv 0.38 0.010 1.000 1 2017 2017
dbSNP: rs6908425
rs6908425
8 0.752 0.320 6 20728500 intron variant T/C snv 0.78 0.010 1.000 1 2008 2008
dbSNP: rs9366357
rs9366357
1 1.000 0.080 6 20599397 intron variant C/T snv 0.39 0.33 0.010 < 0.001 1 2015 2015