Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs12898460
LINC02694
0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251
LINC02694
0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 3
rs2239803
HLA-DRA
0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 3
rs279871
GABRA2
0.882 0.080 4 46303716 intron variant T/C snv 0.38 1
rs6943555
AUTS2
0.882 0.080 7 70341037 intron variant T/A snv 0.34 1
rs10196867
CTNNA2
0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs147247472
AGBL4-IT1 ; AGBL4
0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs2133896
ANKS1B
0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs11825659
IGSF9B
0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs1789924
ADH1C
0.925 0.160 4 99353129 upstream gene variant C/G;T snv 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs1614972
ADH1B ; ADH1C
0.925 0.160 4 99336998 intron variant C/T snv 0.38 3
rs1800759
LOC100507053 ; ADH4
0.925 0.120 4 99144358 intron variant T/G snv 0.49 1
rs2727943 0.925 0.080 3 1856289 intergenic variant T/A;C snv 1
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4