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: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.740 1.000 5 2008 2020
dbSNP: rs10811652
rs10811652
4 0.882 0.120 9 22077086 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1333048
rs1333048
24 0.683 0.320 9 22125348 intron variant A/C snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs2383207
rs2383207
22 0.695 0.280 9 22115960 intron variant A/G snv 0.64 0.020 1.000 2 2012 2015
dbSNP: rs10757272
rs10757272
6 0.851 0.160 9 22088261 intron variant C/T snv 0.41 0.010 1.000 1 2019 2019
dbSNP: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs2383206
rs2383206
17 0.742 0.320 9 22115027 intron variant A/G snv 0.49 0.010 1.000 1 2012 2012
dbSNP: rs2811712
rs2811712
5 0.882 0.080 9 21998036 intron variant G/A snv 0.85 0.010 1.000 1 2012 2012
dbSNP: rs3217992
rs3217992
22 0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 0.010 1.000 1 2011 2011
dbSNP: rs518394
rs518394
6 0.827 0.160 9 22019674 intron variant G/C snv 0.30 0.010 1.000 1 2011 2011
dbSNP: rs564398
rs564398
18 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 0.010 1.000 1 2018 2018
dbSNP: rs7865618
rs7865618
11 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.010 1.000 1 2011 2011