Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs11465759
IL23R ; C1orf141
1 67166721 intron variant T/G snv 2.4E-02 4
rs12285095
ZPR1
11 116787315 non coding transcript exon variant T/G snv 9.8E-02 4
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs5185
AGTR1
3 148742185 3 prime UTR variant T/G snv 6.7E-03 2.5E-02 4
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 4
rs780090
GCKR ; FNDC4
0.925 0.120 2 27495607 upstream gene variant T/C;G snv 4
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs11600380 1.000 0.040 11 116799466 intergenic variant T/C snv 6.6E-02 2
rs12258934
NRG3
10 82015079 intron variant T/C snv 5.1E-02 4
rs16957552
BCAR1
16 75235226 missense variant T/C snv 6.8E-03 2.8E-02 4
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 4
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs4402881
GLB1
3 33012839 intron variant T/C snv 0.93 2
rs480823
LINC02702
11 116655013 intron variant T/C snv 7.3E-02 4
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6