Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs62434129
PLEKHG1
6 150687701 intron variant A/G;T snv 8.8E-02 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 6
rs112233623
CCND3
6 41957260 intron variant C/T snv 7.0E-03 5
rs1126930
PRKAG1 ; DDN-AS1
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 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
rs61745454
CCDC69
5 151187456 missense variant A/G snv 3.7E-02 4.6E-02 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs72959041
RSPO3
6 127133748 intron variant G/A snv 3.2E-02 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