Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7288670
GGT5
22 24225858 intron variant A/C;G snv 4
rs10980797
LOC105376219
9 111150273 intron variant A/G;T snv 3
rs113760175
CASC15
6 22343363 intron variant G/A;T snv 3
rs11642657 16 85982722 intron variant C/A;T snv 3
rs117758012
HOOK2 ; MAST1
1.000 0.080 19 12846836 intron variant C/T snv 4.1E-02 3
rs12459847
MARK4
19 45247899 intron variant G/C snv 0.19 3
rs1991866
CCDC26
8 129611859 intron variant G/A;C snv 3
rs2238783
ARVCF
22 19984929 intron variant C/G snv 0.42 3
rs2615061
LOC102723834
1 225708104 intron variant G/A snv 0.12 3
rs28722705
ANKRD55
5 56158115 intron variant A/T snv 9.9E-02 3
rs73057397
DAGLB ; KDELR2
7 6464609 intron variant T/C snv 0.43 3
rs10098310
CCDC26
8 129601368 intron variant G/A;T snv 2
rs10147992
STXBP6
14 25034593 intron variant A/G;T snv 2
rs10168795
DOCK10
2 224888625 intron variant A/G snv 0.24 2
rs1037171
CD300LF ; RAB37
17 74706839 intron variant G/A snv 0.53 2
rs10562650
ITGA4
2 181459460 intron variant TT/-;T;TTT delins 0.56 2
rs10956483
CCDC26
8 129559864 intron variant G/A;C snv 2
rs10980800
LOC105376219
9 111153625 intron variant T/C snv 0.21 2
rs1105527
KSR1
17 27521170 intron variant C/T snv 0.65 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
rs115007843
SCD5
4 82654059 intron variant A/C snv 0.18 2
rs115340020
RPAP2 ; GLMN
1 92300881 intron variant G/A snv 1.7E-02 2