Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12459507
DOT1L
19 2224388 intron variant A/C snv 0.17 1
rs12635574
FGD5
3 14913042 intron variant A/C snv 0.74 1
rs12916871
CCDC33
15 74260401 intron variant A/C snv 0.28 1
rs13286845
LOC105375990
9 22934664 intron variant A/C snv 0.60 1
rs13431149
LOC105374690 ; MIR217HG
2 55966530 intron variant A/C snv 0.64 1
rs138834
BRD1
22 49786849 intron variant A/C snv 0.22 1
rs141212865
HIPK2
7 139704867 intron variant A/C snv 0.36 1
rs17722107
SH3TC2
5 148982059 intron variant A/C snv 0.16 1
rs2281226
UBE2I
16 1314766 non coding transcript exon variant A/C snv 0.54 1
rs2354862 8 63589186 non coding transcript exon variant A/C snv 0.25 1
rs2594992
ATG7
3 11319523 intron variant A/C snv 0.27 1
rs28708888 15 41606687 downstream gene variant A/C snv 0.27 1
rs302714
RERE ; RERE-AS1
1 8426071 intron variant A/C snv 0.27 1
rs35300112 16 60625908 intergenic variant A/C snv 0.24 1
rs373894
SWAP70
11 9741547 non coding transcript exon variant A/C snv 0.30 1
rs3867466
ALG9
11 111797532 intron variant A/C snv 0.26 1
rs4594837
EBF1
5 158840966 intron variant A/C snv 0.38 1
rs4665624
KLHL29
2 23653120 intron variant A/C snv 0.31 1
rs57954239 18 50746266 intergenic variant A/C snv 0.12 1
rs6771707
GRM7
3 7446201 intron variant A/C snv 0.36 1
rs711737 3 27502164 intergenic variant A/C snv 0.37 1
rs7128382
PAFAH1B2
11 117152771 intron variant A/C snv 0.76 1
rs73074830 3 49539584 downstream gene variant A/C snv 0.11 1
rs7514579
BCAR3
1 93585793 intron variant A/C snv 0.30 1
rs7601101
THSD7B
2 137637029 intron variant A/C snv 0.39 1