Disease: Triglycerides measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17237820
AGTR2
X 116174483 3 prime UTR variant A/T snv 5.7E-03 3
rs6000582
IL2RB
22 37151454 intron variant G/T snv 3.8E-02 3
rs8138057
PDXP
22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs4810479 1.000 0.040 20 45916409 upstream gene variant C/T snv 0.68 4
rs6065904
PLTP
1.000 0.080 20 45906012 intron variant G/A snv 0.23 4
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 4
rs6073952
PLTP
20 45908293 intron variant G/A snv 0.14 4
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 6
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs34338511
NOTCH3
19 15184354 missense variant G/A;T snv 6.1E-04; 4.0E-06 3
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs11873890
TYMS
18 662135 intron variant A/G snv 8.2E-03 3.2E-02 4
rs4987867
BCL2
18 63123839 3 prime UTR variant C/T snv 6.4E-03 3
rs8086463
NPC1 ; RMC1
18 23532038 3 prime UTR variant A/G snv 1.1E-02 3
rs7212502
SLC6A4
17 30222184 intron variant A/G snv 3.2E-02 3
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs17231506
CETP
0.851 0.040 16 56960616 upstream gene variant C/G;T snv 0.28 5