Disease: Low density lipoprotein cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs28917504
CD4
12 6814956 missense variant A/G snv 1.5E-03 6.4E-03 4
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs3999089
JMJD1C
10 63444048 intron variant A/G snv 0.41 2
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs4385188
CERT1
5 75438537 intron variant A/G snv 0.33 4
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs492602
LOC105447645 ; FUT2
0.925 0.120 19 48703160 synonymous variant A/G snv 0.38 0.45 7
rs4969183
PGS1
17 78397291 intron variant A/G snv 0.46 5
rs5020
SLC4A1
17 44255219 splice region variant A/G snv 3.2E-03 1.3E-02 3
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs611917
CELSR2
1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 5
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs6831256
DOK7
4 3471412 intron variant A/G snv 0.49 4
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs721772
RPAP1
15 41537032 synonymous variant A/G snv 0.48 0.42 4
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs77147124
GPAM
10 112159366 intron variant A/G snv 4