Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs174548
FADS2 ; FADS1
0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 6
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs4820268
TMPRSS6
0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 5
rs62160676
MIR4435-2HG
2 111410354 intron variant T/C;G snv 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs113700287
THRB
3 24293020 intron variant -/GTT delins 4
rs11756659 6 25933704 upstream gene variant A/G;T snv 4
rs13335629
FAM234A
16 260381 intron variant G/A;C snv 1.1E-02 4
rs144204502
TK1 ; AFMID
17 78187152 5 prime UTR variant C/G;T snv 1.2E-02 4
rs159058
NOL4L ; LOC101929698
20 32520305 intron variant A/C;T snv 4