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
rs4564803 2 20982630 intergenic variant G/T snv 0.25 5
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 6
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs4850047 2 3587163 regulatory region variant T/C snv 0.84 4
rs506585 2 21174310 intergenic variant G/A;C;T snv 4
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs541041 2 21072103 intergenic variant G/A snv 0.71 3
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs563290 2 21065354 intergenic variant G/A snv 0.69 4
rs668948 1.000 0.040 2 21068657 regulatory region variant G/A snv 0.71 4
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs6736017
PSMD1 ; HTR2B
2 231108702 missense variant T/C snv 6.3E-03 2.5E-02 4
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs754523 2 21088819 intergenic variant A/G snv 0.28 4
rs754524 2 21088669 intergenic variant T/G snv 0.19 4
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8176445
TFPI ; LOC105373786
2 187498080 intron variant T/C snv 8.7E-03 4
rs934198 2 21055901 intergenic variant G/T snv 0.26 3
rs11925396 3 194391622 downstream gene variant A/G snv 1.9E-02 3
rs12721235
AGTR1
3 148722587 intron variant C/A snv 1.7E-02 4
rs2062432
ADCY5
3 123359232 intron variant G/A snv 0.43 4
rs4683438
LOC100507389
3 142933717 non coding transcript exon variant G/T snv 0.33 4