Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 6
rs6993442 8 129683891 upstream gene variant G/C snv 0.17 5
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 5
rs61745454
CCDC69
5 151187456 missense variant A/G snv 3.7E-02 4.6E-02 5
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 5
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 5
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs9880192 1.000 0.040 3 128578726 upstream gene variant G/A;C snv 0.31 4
rs1700159
ACVRL1
1.000 0.040 12 51912002 intron variant C/A;G;T snv 4
rs11327184
CCDC26
8 129592027 intron variant C/- delins 0.40 4
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53 4
rs45577137
CEBPD
8 47739071 upstream gene variant A/G;T snv 4
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 4
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs4432538
PLCB1 ; LOC105372521
20 8626746 intron variant G/A snv 0.52 4
rs72699818
RIN3
14 92611266 intron variant T/C snv 0.12 4