Disease: Triglycerides measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7827408
VPS13B
8 99527615 intron variant C/T snv 2.3E-02 3
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs5743316
TLR3
4 186082537 missense variant A/T snv 4.0E-05 3.5E-05 3
rs11466654
TLR10
4 38774508 synonymous variant T/C;G snv 1.1E-03; 1.8E-05 4
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs9838771
TGFBR2 ; LOC105377016
3 30657290 intron variant G/A snv 2.5E-02 3
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs8176445
TFPI ; LOC105373786
2 187498080 intron variant T/C snv 8.7E-03 4
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs1859287
SUGP1
19 19311378 intron variant T/A;C;G snv 4
rs2023883
SUGP1
19 19294671 intron variant G/A snv 0.19 4
rs2321168
STARD13 ; STARD13-AS
13 33279354 non coding transcript exon variant G/A snv 0.98 4
rs11193085
SORCS1
10 106873848 intron variant G/A snv 8.8E-02 3
rs5020
SLC4A1
17 44255219 splice region variant A/G snv 3.2E-03 1.3E-02 3
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs6736017
PSMD1 ; HTR2B
2 231108702 missense variant T/C snv 6.3E-03 2.5E-02 4
rs10504062
PRKDC
8 47824663 intron variant T/C snv 2.1E-02 3
rs9658150
PPARD
6 35420123 splice region variant G/A snv 3.6E-05 5.6E-05 3
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs8138057
PDXP
22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6