Disease: C-reactive protein measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 7
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 4
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 4
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs157595 1.000 0.080 19 44922203 upstream gene variant A/G;T snv 3
rs1936797 6 127111512 intron variant A/G snv 0.33 3
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 3
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3
rs11874381
LOC105372112
18 49677038 intergenic variant G/A snv 0.32 2
rs12742376
KDF1
1 26958704 intron variant C/T snv 6.8E-02 2