Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4665963
TRIM54
0.925 0.120 2 27305824 splice region variant T/C snv 0.35 0.43 3
rs1049817
GTF3C2
0.925 0.120 2 27328100 synonymous variant A/G snv 0.42 0.48 3
rs7586601 0.925 0.120 2 27361799 intron variant A/G snv 0.54 3
rs1528533
SNX17
0.925 0.120 2 27372889 non coding transcript exon variant G/C snv 0.47 3
rs13472
ZNF513 ; SNX17
0.925 0.120 2 27377372 3 prime UTR variant G/A snv 0.38 3
rs780090
GCKR ; FNDC4
0.925 0.120 2 27495607 upstream gene variant T/C;G snv 4
rs813592
GCKR
0.925 0.120 2 27499104 intron variant T/C snv 0.42 0.47 3
rs2293572
GCKR
0.925 0.120 2 27505910 intron variant C/G snv 0.39 3
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
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5
rs814295
GCKR
0.925 0.120 2 27520348 intron variant A/G snv 0.18 5
rs11681351
GCKR
0.925 0.120 2 27520556 intron variant G/A snv 0.36 3
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 8
rs1919127
C2orf16
0.925 0.120 2 27578626 missense variant T/C snv 0.31 0.27 6
rs1919128
C2orf16
0.882 0.120 2 27578892 missense variant A/G snv 0.30 0.24 6
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs3749147
GPN1 ; CCDC121
0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 6
rs13030345
MRPL33
0.925 0.120 2 27780307 intron variant G/T snv 0.15 3
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 5
rs2240466
BAZ1B
0.925 0.120 7 73441939 3 prime UTR variant G/A snv 9.2E-02 4
rs1178979
BAZ1B
0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21 6
rs714052
BAZ1B
0.925 0.120 7 73450539 intron variant A/G snv 9.2E-02 4