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 0.810 1.000 3 2012 2012
dbSNP: rs4977756
rs4977756
24 0.683 0.440 9 22068653 intron variant G/A snv 0.64 0.810 1.000 3 2011 2014
dbSNP: rs10811645
rs10811645
2 1.000 0.040 9 22049657 intron variant G/A snv 0.59 0.800 1.000 2 2012 2018
dbSNP: rs1333037
rs1333037
3 0.925 0.040 9 22040766 intron variant C/T snv 0.71 0.800 1.000 2 2012 2018
dbSNP: rs2157719
rs2157719
17 0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 0.800 1.000 2 2012 2015
dbSNP: rs7865618
rs7865618
11 0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 0.800 1.000 2 2012 2012
dbSNP: rs7866783
rs7866783
2 1.000 0.040 9 22056360 non coding transcript exon variant A/G snv 0.71 0.800 1.000 2 2012 2016
dbSNP: rs944800
rs944800
1 1.000 0.040 9 22050899 intron variant A/G snv 0.78 0.800 1.000 2 2012 2018
dbSNP: rs944801
rs944801
4 0.882 0.120 9 22051671 intron variant G/A;C snv 0.800 1.000 2 2012 2018
dbSNP: rs523096
rs523096
7 0.827 0.080 9 22019130 intron variant A/G snv 0.30 0.710 1.000 3 2012 2012
dbSNP: rs10965219
rs10965219
4 0.882 0.080 9 22053688 intron variant A/G snv 0.58 0.700 1.000 2 2012 2012
dbSNP: rs518394
rs518394
6 0.827 0.160 9 22019674 intron variant G/C snv 0.30 0.700 1.000 2 2012 2012
dbSNP: rs564398
rs564398
18 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 0.700 1.000 2 2012 2012
dbSNP: rs8181047
rs8181047
7 0.807 0.120 9 22064466 intron variant A/G snv 0.79 0.700 1.000 2 2012 2012
dbSNP: rs1008878
rs1008878
2 1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 0.700 1.000 1 2012 2012
dbSNP: rs10115049
rs10115049
2 1.000 0.040 9 22032120 intron variant A/G snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.700 1.000 1 2012 2012
dbSNP: rs10120688
rs10120688
7 0.807 0.080 9 22056500 intron variant G/A snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs10120806
rs10120806
1 1.000 0.040 9 22047946 intron variant T/C snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs10738604
rs10738604
3 1.000 0.040 9 22025494 intron variant G/A snv 0.29 0.700 1.000 1 2012 2012
dbSNP: rs10738605
rs10738605
3 0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs10757263
rs10757263
1 1.000 0.040 9 22013806 non coding transcript exon variant C/T snv 0.56 0.700 1.000 1 2012 2012
dbSNP: rs10757265
rs10757265
2 1.000 0.040 9 22048860 intron variant T/C snv 0.49 0.700 1.000 1 2012 2012
dbSNP: rs10757266
rs10757266
1 1.000 0.040 9 22049556 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10757267
rs10757267
2 1.000 0.040 9 22052811 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012