Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 4
rs61823972
TMCC2
1 205232197 intron variant A/C;T snv 4
rs739385 7 93053295 regulatory region 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
rs1211375
LUC7L
1.000 0.040 16 190281 intron variant A/C;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
rs4832312
RMND5A
2 86762839 intron variant G/A;C snv 3
rs496321
LOC101929295
11 95153468 intron variant T/C;G snv 3
rs5831579
LOC102724142
2 60402304 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC delins 3
rs643381 6 139518286 intron variant C/A;G snv 3
rs6538148 12 88424702 intergenic variant C/G;T snv 3
rs6569992 6 135131014 intergenic variant G/A;C;T snv 3
rs747844459 6 36634250 regulatory region variant C/G;T snv 3
rs875741 5 173860848 intergenic variant G/A;C snv 3
rs9924561
FAM234A
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 3
rs10751450
ATP2B4
1 203681817 intron variant C/G;T snv 2
rs10783487
ATG101
12 52068035 upstream gene variant G/A;T snv 2
rs1134634
CC2D2A
4 15601446 3 prime UTR variant G/C;T snv 0.58; 9.4E-06 2
rs11669479
HDGFL2
19 4485049 intron variant A/G;T snv 2
rs1203039
RAB11FIP3
16 461337 intron variant G/A;C snv 2
rs12232375
ZFPM1
16 88500003 intron variant G/A;C;T snv 2