Disease: C-reactive protein measurement
Source: GWASDB ×
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 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs9987289
LOC157273
1.000 0.040 8 9325848 non coding transcript exon variant A/G snv 0.87 8
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 3