Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs174566
FADS1 ; FADS2
0.925 0.160 11 61824890 intron variant A/G snv 0.34 7
rs174554
FADS1 ; FADS2
1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 6
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 5
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 5
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 5
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 5