Disease: Low density lipoprotein cholesterol measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 7
rs17398765 2 21047879 upstream gene variant A/G snv 4.8E-02 3
rs17646665
SORT1
1.000 0.080 1 109369429 intron variant A/G snv 5.8E-02 3
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs17884841
MMP14
14 22843265 missense variant A/G snv 1.9E-03 7.2E-03 3
rs1800481
APOB
2 21044338 upstream gene variant A/G snv 0.82 3
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
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2182833 1 55034756 upstream gene variant A/G snv 0.23 3
rs2495477
PCSK9
1 55052794 splice region variant A/G snv 0.42 0.49 3
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 7
rs2738452
LDLR
19 11118542 intron variant A/G snv 0.34 3
rs28917504
CD4
12 6814956 missense variant A/G snv 1.5E-03 6.4E-03 4
rs3093208
CYP4F2
19 15877772 downstream gene variant A/G snv 4.0E-02 3
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs34131586
CNTF ; ZFP91-CNTF
11 58622865 missense variant A/G snv 2.8E-05 4.2E-05 3
rs34998951
VLDLR-AS1 ; VLDLR
9 2634144 intron variant A/G snv 6.7E-03 3
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs3780181
VLDLR-AS1 ; VLDLR
1.000 0.320 9 2640759 intron variant A/G snv 0.11 3
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs4253642
LOC105373074 ; PPARA
22 46167520 intron variant A/G snv 7.1E-03 5
rs4385188
CERT1
5 75438537 intron variant A/G snv 0.33 4