Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17023459
AFF3
2 100067088 intron variant C/A;T snv 1
rs9557386
PCCA
13 100115087 intron variant C/G snv 0.33 1
rs6709656
AFF3
2 100190257 intron variant A/G snv 0.29 1
rs2309757
AFF3
2 100191263 intron variant T/C snv 0.29 1
rs71413877
LONRF2
2 100308360 intron variant G/A snv 2.6E-02 2
rs10183150
LONRF2
2 100322655 upstream gene variant A/G;T snv 1
rs10164820 2 100433891 intergenic variant G/C snv 0.20 1
rs34106693 2 100535368 intergenic variant C/G snv 0.11 1
rs9513780
TMTC4
13 100666927 intron variant C/T snv 0.37 1
rs2942884 2 100707116 regulatory region variant G/A snv 0.50 1
rs1693584
LOC105375673
8 100736689 downstream gene variant T/C snv 0.28 1
rs4906037
LOC105370670
14 101076143 splice region variant T/C snv 0.71 1
rs6421896 5 101205761 intergenic variant A/G snv 0.71 1
rs72776049
GRIN2A
16 10127597 intron variant T/C snv 0.24 1
rs58764043
MSRA
8 10148373 intron variant C/T snv 0.20 1
rs6575858 14 101565415 upstream gene variant C/G;T snv 1
rs2895917 14 101586438 intergenic variant C/T snv 0.32 1
rs12380816
GRIN3A
9 101651388 intron variant T/C snv 0.20 1
rs1337415
GRIK2
6 101664650 intron variant A/G;T snv 1
rs749694
LOC105378458
10 101760027 regulatory region variant A/G snv 0.45 2
rs2529207 7 101780519 intergenic variant C/T snv 0.32 1
rs2735421
NPM3 ; FGF8
10 101781259 upstream gene variant T/G snv 0.65 2
rs8046217 16 10195005 intergenic variant T/A snv 0.13 1
rs401966
CUX1
7 102052537 intron variant C/G;T snv 1
rs61874768
LDB1 ; PPRC1
10 102120361 5 prime UTR variant G/A;T snv 2