Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs72737330
ESRRG
0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs11825659
IGSF9B
0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs12544026
NCALD
0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs11681792
NRXN1
1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs79246196
STAG3
0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs1437396 1.000 0.080 2 55278320 upstream gene variant C/G;T snv 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3
rs17125651 1.000 0.080 10 109063325 intergenic variant T/C snv 0.14 3
rs2168784 1.000 0.080 3 164872151 intergenic variant C/T snv 0.24 3
rs4699741 1.000 0.080 4 99357540 upstream gene variant T/C snv 9.2E-02 3
rs4715221 1.000 0.080 6 51495005 regulatory region variant G/A;C;T snv 3
rs4936277 1.000 0.080 11 113561238 intergenic variant A/G snv 0.37 3
rs540606 1.000 0.080 2 44911368 intergenic variant A/G snv 0.66 3
rs570436 1.000 0.080 2 44915534 intergenic variant C/T snv 0.69 3
rs61776290 1.000 0.080 1 10634850 upstream gene variant C/T snv 8.7E-02 3
rs61902812 1.000 0.080 11 113503698 intergenic variant C/A snv 0.26 3
rs6701037 1.000 0.080 1 175150943 downstream gene variant A/C;T snv 3
rs6777876 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 3