Disease: Triglycerides 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
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs1129555
GPAM
10 112150963 3 prime UTR variant A/G snv 0.71 5
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs2247056
LOC112267902 ; HLA-B ; LINC02571
0.882 0.160 6 31297713 intron variant T/C snv 0.80 4
rs5112
APOC1P1
1.000 0.080 19 44927023 non coding transcript exon variant C/G snv 0.55 4
rs59950280
LOC105374354
4 3450618 upstream gene variant G/A snv 0.41 4
rs7916868
JMJD1C
10 63229171 intron variant A/T snv 0.47 3
rs2395655
CDKN1A ; DINOL
0.882 0.120 6 36677919 5 prime UTR variant A/G snv 0.43 0.49 2
rs35665085
HDHD5
22 17145025 missense variant G/A snv 4.1E-02 3.8E-02 2