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: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.050 0.800 5 2011 2017
dbSNP: rs10120688
rs10120688
7 0.807 0.080 9 22056500 intron variant G/A snv 0.50 0.030 1.000 3 2012 2014
dbSNP: rs2157719
rs2157719
17 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 0.030 1.000 3 2012 2018
dbSNP: rs1011970
rs1011970
22 0.677 0.320 9 22062135 intron variant G/T snv 0.23 0.010 1.000 1 2014 2014
dbSNP: rs2383204
rs2383204
6 0.827 0.160 9 22055049 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs523096
rs523096
7 0.827 0.080 9 22019130 intron variant A/G snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs7049105
rs7049105
7 0.807 0.120 9 22028802 intron variant A/G snv 0.58 0.010 1.000 1 2012 2012