Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs35436 1.000 0.080 12 115116718 intergenic variant C/T snv 0.40 5
rs12130333 1.000 0.080 1 62726106 regulatory region variant C/T snv 0.16 4
rs3212335
GABRB3 ; LOC112268151
1.000 0.080 15 26766994 intron variant C/T snv 0.32 4
rs1052053
PMF1 ; PMF1-BGLAP
1.000 0.080 1 156232382 missense variant A/C;G snv 1.0E-03; 0.38 3
rs12204590
LOC112267978 ; LINC01394
1.000 0.080 6 1337158 intergenic variant T/A snv 0.14 3
rs12476527
KCNK3
1.000 0.080 2 26692756 5 prime UTR variant G/C;T snv 3
rs147783135
TMPRSS7
1.000 0.080 3 112081004 stop gained C/T snv 2.4E-04 6.3E-05 3
rs191885206
CYP4F12
1.000 0.080 19 15696024 missense variant T/C snv 7.0E-04 3.1E-04 3
rs2005108 1.000 0.080 11 102899623 downstream gene variant C/G;T snv 3
rs2292661
PDIA5
1.000 0.080 3 123150263 missense variant C/G;T snv 8.2E-04 3
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs42039
CDK6
1.000 0.080 7 92615108 3 prime UTR variant C/T snv 0.19 0.19 3
rs4471613
ALDH1A2
1.000 0.080 15 58259495 intron variant G/A snv 4.3E-02 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs768349387
ADRB2
1.000 0.080 5 148827850 missense variant T/C snv 8.0E-06 3
rs7859727
CDKN2B-AS1
1.000 0.080 9 22102166 intron variant C/T snv 0.57 3
rs867671924
ITGB3
1.000 0.080 17 47292176 missense variant C/A snv 3
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 3
rs10435816
IL33
1.000 0.080 9 6225535 intron variant A/G snv 0.35 2
rs10947803
KCNK17
1.000 0.080 6 39302834 intron variant C/A snv 2
rs11018628
NOX4
1.000 0.080 11 89473343 intron variant T/C;G snv 2
rs11196288 1.000 0.080 10 113297684 regulatory region variant A/G snv 5.5E-02 2
rs11237379
NDUFC2-KCTD14 ; NDUFC2
1.000 0.080 11 78074911 intron variant T/C snv 0.38 2
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 2