Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34325700 8 42673524 intergenic variant -/A delins 1
rs200049096
HYKK
15 78510715 intron variant -/T delins 1.4E-05 1
rs6495314
CHRNB4 ; LOC112268142
0.925 0.080 15 78668187 intron variant A/C snv 0.35 3
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 2
rs1028936
HECTD2-AS1
10 91590040 regulatory region variant A/C snv 0.18 1
rs11072811
MORF4L1
1.000 0.040 15 78839988 intron variant A/C snv 0.51 1
rs1396618
NRXN3
14 78825561 intron variant A/C snv 9.9E-02 1
rs1979905
PSMA4
15 78550032 3 prime UTR variant A/C snv 0.66 1
rs2656052
IREB2
15 78448590 intron variant A/C snv 0.36 1
rs7017612 8 42744102 regulatory region variant A/C snv 0.36 1
rs7506051
ZNF407
18 74589381 downstream gene variant A/C snv 0.72 1
rs7837296 8 42671751 intergenic variant A/C snv 0.70 1
rs215601
PDE1C
7 32294309 intron variant A/C;G snv 1
rs6463923 7 9531372 intergenic variant A/C;G snv 1
rs7004381
LOC105379396 ; CHRNB3
8 42696018 upstream gene variant A/C;G snv 1
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 1
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 3
rs11205277 1.000 0.120 1 149920979 upstream gene variant A/C;G;T snv 1
rs12903295
IREB2
15 78486630 intron variant A/C;G;T snv 1
rs7773004 1.000 0.040 6 26267527 downstream gene variant A/C;G;T snv 1
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs6474414
CHRNB3
8 42705193 intron variant A/C;T snv 1
rs7778788
PDE1C
7 32307362 intron variant A/C;T snv 1
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 1