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
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2954022 8 125470379 intron variant C/A;T snv 4
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs4360309 8 125511281 intron variant C/G;T snv 3
rs10986881
PBX3
9 125756807 intron variant C/T snv 1.8E-02 3
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs7100433
ECHS1
10 133370298 intron variant T/C snv 0.98 3
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs4683438
LOC100507389
3 142933717 non coding transcript exon variant G/T snv 0.33 4
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs5185
AGTR1
3 148742185 3 prime UTR variant T/G snv 6.7E-03 2.5E-02 4
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs6855363 4 156749385 intergenic variant T/A;C snv 4
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9