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
rs7993724
PDX1 ; PLUT
13 27919139 upstream gene variant T/C snv 5.6E-03 6
rs8071787
GAS7
17 10058819 intron variant T/C snv 4.8E-02 5
rs8176445
TFPI ; LOC105373786
2 187498080 intron variant T/C snv 8.7E-03 4
rs9658736
FAS
10 89004160 intron variant T/C snv 9.4E-03 3
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs1859287
SUGP1
19 19311378 intron variant T/A;C;G snv 4
rs12047226
DOCK7
1 62639867 intron variant T/A;C snv 4
rs17789218
LOC105377911
6 100152221 intergenic variant T/A;C snv 3
rs6855363 4 156749385 intergenic variant T/A;C snv 4
rs7951347
CSRP3 ; CSRP3-AS1
11 19198031 intron variant T/A;C snv 3
rs17883880
CHUK
10 100230590 intron variant T/A snv 1.2E-02 4
rs2285628
MAU2
19 19357187 3 prime UTR variant T/A snv 0.22 4
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs283813
NECTIN2
1.000 0.080 19 44885917 intron variant T/A snv 0.11 0.16 6
rs74664507 1.000 0.040 9 16913838 upstream gene variant T/A snv 3
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs2131925
DOCK7
1 62560271 intron variant G/T snv 0.57 6
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs4564803 2 20982630 intergenic variant G/T snv 0.25 5
rs4683438
LOC100507389
3 142933717 non coding transcript exon variant G/T snv 0.33 4
rs567279
PDE4B
1 66222346 intron variant G/T snv 0.97 4
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15