Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61745454
CCDC69
5 151187456 missense variant A/G snv 3.7E-02 4.6E-02 5
rs34557412
TNFRSF13B
0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs475616 10 30207976 regulatory region variant A/G snv 0.67 3
rs75963851 11 95363157 intergenic variant A/G snv 3.1E-03 3
rs7826487 8 7023403 regulatory region variant A/G snv 0.17 3
rs10168795
DOCK10
2 224888625 intron variant A/G snv 0.24 2
rs11189181
RRP12
10 97384397 intron variant A/G snv 0.30 2
rs114208039
HLA-B ; HLA-C
6 31273862 intron variant A/G snv 2
rs12346772
LOC105376219
9 111158319 intron variant A/G snv 0.18 2
rs13022141 2 136131638 intergenic variant A/G snv 0.69 2
rs140058837 3 46313128 upstream gene variant A/G snv 2.2E-02 2
rs1400745 14 34886094 intergenic variant A/G snv 0.41 2
rs17485419
LOC105375911
8 78232042 regulatory region variant A/G snv 0.23 2
rs17739167
EHD4
15 41942834 non coding transcript exon variant A/G snv 0.41 2
rs200516372 3 141484141 upstream gene variant A/G snv 2.4E-02 2
rs35493131
ERF
19 42248882 synonymous variant A/G snv 9.7E-02 8.9E-02 2
rs35928002
ARRDC2
19 18005335 intron variant A/G snv 0.45 2
rs360017
LINC01485 ; LOC107986482
5 173780350 non coding transcript exon variant A/G snv 0.83 2
rs3931
NOSTRIN ; SPC25
2 168864871 synonymous variant A/G snv 4.0E-06; 0.27 0.25 2
rs4142441
OSER1-DT ; OSER1
20 44210980 non coding transcript exon variant A/G snv 0.15 2
rs4385425 7 50267738 upstream gene variant A/G snv 0.40 2
rs4812447
LOC102724968
20 40643980 regulatory region variant A/G snv 0.51 2
rs58681483 17 59857293 downstream gene variant A/G snv 0.13 2
rs62396356
TREML2
6 41200025 intron variant A/G snv 9.0E-02 2