Disease: C-reactive protein measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
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
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 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
rs174546
FADS1 ; FADS2
0.807 0.200 11 61802358 3 prime UTR variant C/T snv 0.28 7
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs1160985
TOMM40
1.000 0.080 19 44900155 intron variant C/T snv 0.52 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 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
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 3
rs1529711
CARM1
1.000 0.080 19 10912758 intron variant C/T snv 0.13 3
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 3
rs340025
RORA ; RORA-AS1
15 60616108 intron variant T/A;C snv 3
rs3822857
FRK
6 115992768 intron variant G/A;C snv 3
rs4703642
LOC105379040
5 74966337 intron variant A/G snv 0.50 3