Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2133896
ANKS1B
0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs4699741 1.000 0.080 4 99357540 upstream gene variant T/C snv 9.2E-02 3
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs12639833
ADH1C ; ADH1B
1.000 0.080 4 99346215 intron variant C/T snv 0.31 3
rs2241894
ADH1C ; ADH1B
1.000 0.080 4 99344976 synonymous variant T/A;C snv 4.0E-06; 0.30 3
rs1614972
ADH1B ; ADH1C
0.925 0.160 4 99336998 intron variant C/T snv 0.38 3
rs1612735
ADH1B ; ADH1C
1.000 0.080 4 99336850 intron variant T/C snv 0.31 3
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs2173201
ADH1B
1.000 0.080 4 99329813 intron variant C/A snv 0.30 3
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs2075633
ADH1B
1.000 0.080 4 99317841 non coding transcript exon variant T/C snv 0.24 3
rs1693457
ADH1B
1.000 0.080 4 99315605 non coding transcript exon variant C/T snv 0.81 3
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 3
rs904092
LOC100507053
1.000 0.080 4 99293007 intron variant A/G;T snv 3
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1800759
LOC100507053 ; ADH4
0.925 0.120 4 99144358 intron variant T/G snv 0.49 1
rs5860563
ADH4 ; LOC100507053
1.000 0.080 4 99126006 intron variant -/A delins 3
rs72900220
LOC112267901
1.000 0.080 4 98671846 intergenic variant A/G snv 1.3E-02 3
rs7913179 1.000 0.080 10 97705109 intergenic variant C/A;G;T snv 3
rs9556711
MBNL2
1.000 0.080 13 97364162 intron variant G/A snv 0.20 3
rs11922615
SETD5
1.000 0.080 3 9416623 intron variant A/G snv 8.4E-02 1
rs6443238
SETD5
1.000 0.080 3 9407371 intron variant C/T snv 8.4E-02 1
rs8040009
C15orf32
1.000 0.080 15 92501109 non coding transcript exon variant T/C;G snv 3