Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 4
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3
rs1490384 6 126530014 intron variant C/G;T snv 3
rs1688043
HPN-AS1 ; HPN
19 35062437 intron variant C/G;T snv 3
rs1936797 6 127111512 intron variant A/G snv 0.33 3
rs2710804 7 36044919 intron variant T/C snv 0.29 3
rs340005
RORA-AS1 ; RORA
15 60585831 intron variant G/A snv 0.67 3
rs340025
RORA ; RORA-AS1
15 60616108 intron variant T/A;C snv 3
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3
rs643434
ABO
9 133266942 intron variant A/G;T snv 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs7012637 8 9315699 intron variant G/A;C snv 3
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3