Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs984222
TBX15
1 118961220 intron variant C/A;G snv 3
rs9837325
PLXND1
3 129596988 intron variant C/A snv 0.22 1
rs982085
REEP2
5 138439892 intron variant C/G snv 0.58 1
rs9818103 3 35630453 intergenic variant A/G snv 0.30 1
rs9798015
MEIS1
2 66541130 intron variant C/T snv 0.33 1
rs9792666
LOC105376197
9 105125457 intron variant A/G snv 5.2E-02 1
rs9791192 6 127221808 intergenic variant C/T snv 0.19 1
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs974801
TET2
4 105149907 intron variant A/G snv 0.36 1
rs9742
CDC42EP3
2 37642351 3 prime UTR variant G/A;T snv 1
rs9678859
AFF3
2 99672016 intron variant A/G snv 0.84 1
rs9668760 12 34458237 intergenic variant C/A;G;T snv 1
rs9659380
DPYD ; MIR137HG
1 97957593 intron variant G/A snv 0.84 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 2
rs9644033
LOC107986930
8 23753126 intron variant A/T snv 0.25 1
rs9630986
SCHLAP1
2 180743024 intron variant G/C;T snv 1
rs9596077
CDADC1
13 49274697 intron variant G/A snv 0.61 1
rs9583489
COL4A2
13 110380486 intron variant C/T snv 0.27 1
rs9557704
ITGBL1
13 101575144 intron variant A/G;T snv 1
rs9555695
COL4A2
13 110380778 intron variant C/T snv 0.36 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs951252
ANAPC10
4 144903999 intron variant A/G;T snv 0.63 2
rs950732 10 92354876 downstream gene variant C/T snv 0.55 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 2