Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs79220007
HFE
6 26098246 3 prime UTR variant T/C snv 3.8E-02 5
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 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
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
rs12459419
CD33
0.925 0.120 19 51225221 missense variant C/G;T snv 0.31 4
rs12764899
AS3MT ; BORCS7-ASMT
1.000 0.040 10 102875346 intron variant G/A snv 0.21 4
rs12777
MIR3936HG ; SLC22A4
5 132335969 synonymous variant C/G snv 3.1E-02 2.8E-02 4
rs142529006
ZKSCAN1
7 100022093 intron variant T/A snv 6.9E-03 4
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4
rs148125759
UGCG
9 111901105 intron variant T/C snv 1.0E-02 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4