Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11716413
TRIM59 ; TRIM59-IFT80
3 160458109 intron variant A/C snv 0.21 2
rs12137294 1 205213744 upstream gene variant A/C snv 0.46 2
rs12903987 15 89237741 intergenic variant A/C snv 0.47 2
rs1820934
TM4SF18
3 149329998 non coding transcript exon variant A/C snv 0.62 2
rs2143918
A4GALT
22 42718014 intron variant A/C snv 0.41 2
rs2243547
LIPA
10 89250722 intron variant A/C snv 0.26 2
rs2774952
DIPK1A
1 92889689 intron variant A/C snv 0.68 2
rs4473902
FIG4
6 109799064 intron variant A/C snv 8.9E-02 2
rs4794048
KPNB1
17 47685707 upstream gene variant A/C snv 0.45 2
rs555280966 1 158457418 upstream gene variant A/C snv 8.4E-03 2
rs55861694
SLC12A7
5 1051642 3 prime UTR variant A/C snv 1.1E-02 2
rs58167401
SLC22A23
6 3423353 intron variant A/C snv 5.0E-02 2
rs7245983
CILP2
19 19546823 downstream gene variant A/C snv 0.43 2
rs8176671
ABO
9 133266900 intron variant A/C snv 2
rs9534136
TPT1-AS1
13 45386494 intron variant A/C snv 0.68 2
rs9946510
SMAD7
18 48931857 intron variant A/C snv 0.25 2
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs77960347
LIPG
18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03 5
rs1958078
SMOC1
14 69888141 intron variant A/C;G snv 4
rs754205
IRS2
13 109759295 intron variant A/C;G snv 4
rs13092376
PAK2
3 196789417 intron variant A/C;G snv 0.33 3
rs10503728
SLC25A37
8 23563489 intron variant A/C;G snv 2
rs11117363 16 88086625 intron variant A/C;G snv 2
rs11258564
FRMD4A
10 13730905 intron variant A/C;G snv 2
rs12485168
PARVB
22 44059293 intron variant A/C;G snv 2