Disease: Low density lipoprotein cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs306890
SPRY3
Y 56944005 intergenic variant T/C snv 4
rs6461564
SP4
7 21456809 intron variant T/C snv 0.38 3
rs11193085
SORCS1
10 106873848 intron variant G/A snv 8.8E-02 3
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs5020
SLC4A1
17 44255219 splice region variant A/G snv 3.2E-03 1.3E-02 3
rs12208357
SLC22A1
1.000 0.080 6 160122116 missense variant C/T snv 5.2E-02 4.9E-02 5
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4
rs895953
SETD1B
1.000 0.040 12 121811142 intron variant G/T snv 0.76 5
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs2384034
RPH3A
12 112766880 intron variant C/G;T snv 4
rs721772
RPAP1
15 41537032 synonymous variant A/G snv 0.48 0.42 4
rs7544735
RNU6ATAC35P
1.000 0.040 1 220825571 intron variant G/A snv 0.22 3
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
rs6059932
PIGU
20 34587662 intron variant C/T snv 0.44 4
rs4129767
PGS1
17 78407903 intron variant G/A snv 0.46 6
rs4969183
PGS1
17 78397291 intron variant A/G snv 0.46 5
rs8071884
PGS1
17 78401977 intron variant C/A;G;T snv 4
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
rs7993724
PDX1 ; PLUT
13 27919139 upstream gene variant T/C snv 5.6E-03 6
rs567279
PDE4B
1 66222346 intron variant G/T snv 0.97 4