Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs1028728
POSTN
0.925 0.040 13 37599679 upstream gene variant A/T snv 0.20 3
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs10519210 1.000 0.040 15 63445726 intergenic variant T/C;G snv 1
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10927887
CLCNKA
0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs10932374
ERBB4
0.925 0.040 2 211379678 3 prime UTR variant G/A snv 0.23 2
rs11006544
LOC107984235
1.000 0.040 10 59510886 intergenic variant T/C snv 7.3E-03 3
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs11110004
ANKS1B
1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 3
rs11172782 1.000 0.040 12 58865846 intergenic variant A/G snv 0.12 1
rs112434206 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 3
rs113235453
NUBPL
1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02 3
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs114821210 1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03 3
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 6
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8