Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 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
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 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
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs2074585
IQGAP1
0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67 5
rs34651
TNPO1
1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
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
rs61745454
CCDC69
5 151187456 missense variant A/G snv 3.7E-02 4.6E-02 5
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5