Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 4
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 4
rs2337106
SMAD7
18 48934533 intron variant C/A;G snv 4
rs368865
ATP11A
13 112825506 missense variant A/C;G;T snv 0.76; 4.0E-06 4
rs4712656
CASC15 ; NBAT1
1.000 0.040 6 22136033 non coding transcript exon variant G/A;C snv 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4
rs837763
LOC107984842
16 88787321 upstream gene variant C/G;T snv 4
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 4
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 3
rs115986297
GMDS
6 2050557 intron variant A/C;G snv 3
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;T snv 3
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 3
rs12636078
KAT2B
3 20064181 intron variant A/G;T snv 3
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 3
rs148910659
KANSL1
17 46055293 intron variant G/A snv 3
rs149804345 3 56710234 intergenic variant AACAAA/-;AACAAAAACAAA;AACAAAAACAAAAACAAA delins 3
rs1997595 21 15205839 intron variant A/C;G snv 3
rs218264 4 54542708 intergenic variant A/G;T snv 3
rs366684
PROX1
1 214013919 intron variant G/A;C snv 3
rs496321
LOC101929295
11 95153468 intron variant T/C;G snv 3
rs533281866
EGLN1
1 231422308 intron variant G/A;C snv 3
rs5831579
LOC102724142
2 60402304 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC delins 3
rs609018 12 3962735 regulatory region variant T/A;G snv 3
rs634869 6 139510620 intron variant T/A;C snv 3