Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 5
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs4253642
LOC105373074 ; PPARA
22 46167520 intron variant A/G snv 7.1E-03 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs28917504
CD4
12 6814956 missense variant A/G snv 1.5E-03 6.4E-03 4
rs4385188
CERT1
5 75438537 intron variant A/G snv 0.33 4
rs611917
CELSR2
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4