Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2820464
LYPLAL1-AS1
1 219519878 intergenic variant G/A;C snv 1
rs3088050
NSD1
5 177299634 3 prime UTR variant G/A snv 0.18 1
rs4580892 6 127088737 intron variant C/T snv 0.32 1
rs4640244
KCNJ12
17 21380911 intron variant A/G snv 0.33 1
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 1
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 1
rs4846567 1 219577375 regulatory region variant G/T snv 0.23 1
rs505102
CFH
1 196650372 upstream gene variant T/C snv 0.40 1
rs55747707
MLXIPL
7 73623036 intron variant G/A snv 0.16 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs6486060
NRIP3 ; LOC105376541
11 9003083 intron variant G/A snv 0.55 1
rs6701231
TBX15
1 118953038 intron variant C/A;G snv 1
rs6861681
CPEB4
5 173935455 intron variant G/A snv 0.22 1
rs6931262
RREB1
6 7217284 non coding transcript exon variant C/T snv 0.10 1
rs6942652
CPED1
7 121249218 intron variant G/C;T snv 1
rs7246865
MYO9B
19 17108295 intron variant G/A snv 0.36 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs7745274
RSPO3 ; LOC112267972
6 127188012 intron variant G/A snv 0.56 1
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs12061508 1.000 0.040 1 196615338 intergenic variant G/A snv 0.23 2