Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3768321
PABPC4 ; PABPC4-AS1
1.000 0.080 1 39570256 intron variant G/T snv 0.14 5
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs55709272
IL1RN
2 113109711 intron variant T/A;C snv 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 5
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 5
rs7394579
FADS2 ; FADS1
1.000 0.080 11 61813978 intron variant A/G snv 0.22 5
rs74035509
ZFPM1
16 88500925 intron variant C/T snv 0.10 5
rs755249
PPIEL ; BMP8A
1 39529402 3 prime UTR variant C/A;T snv 5
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs920112
CDCA7
2 173354407 intron variant G/A snv 1.0E-01 5
rs9411378
ABO
9 133270015 intron variant A/C;T snv 5
rs11021221 11 95575690 intron variant T/A;G snv 4
rs112329286
SYNE2
1.000 0.080 14 63773159 intron variant -/ATTT delins 0.24 4
rs11244669
DHX32 ; BCCIP
10 125844213 intron variant A/C snv 0.28 4
rs116577908
PLCL2
3 17056907 intron variant A/G snv 7.1E-03 4
rs1169299
HNF1A
1.000 0.080 12 120991391 intron variant T/C snv 0.43 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs12050884
EIF2AK4
15 40014133 intron variant C/A snv 0.25 4
rs12134279 0.925 0.080 1 197812068 regulatory region variant C/T snv 0.17 4
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4