Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5860563
ADH4 ; LOC100507053
1.000 0.080 4 99126006 intron variant -/A delins 3
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs143894582
PTPN11
1.000 0.080 12 112469070 intron variant A/-;AA delins 1
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 3
rs9378160
MICB
1.000 0.080 6 31500215 intron variant A/C;G snv 3
rs12898370
HMG20A
1.000 0.080 15 77516256 intergenic variant A/C;T snv 3
rs6701037 1.000 0.080 1 175150943 downstream gene variant A/C;T snv 3
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
rs139438618
SEMA3A
0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs1000579
STX18-AS1
1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs10211296
CSRNP3
1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs2002594
FAM162A
1.000 0.080 3 122392714 intron variant A/G snv 0.59 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
rs55768019
LINC02268
1.000 0.080 4 174106365 intron variant A/G snv 0.43 3
rs6777876 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 3
rs72900220
LOC112267901
1.000 0.080 4 98671846 intergenic variant A/G snv 1.3E-02 3
rs750338
PKNOX2
1.000 0.080 11 125302697 intron variant A/G snv 0.30 3
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3
rs904092
LOC100507053
1.000 0.080 4 99293007 intron variant A/G;T snv 3
rs1660895 1.000 0.080 2 129236759 intergenic variant A/T snv 0.52 3