Disease: Serum LDL cholesterol measurement ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs646776
rs646776 		0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 6 2008 2013
dbSNP: rs12740374
rs12740374 		0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 5 2008 2012
dbSNP: rs629301
rs629301 		0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 4 2008 2013
dbSNP: rs660240
rs660240 		1 109275216 3 prime UTR variant T/C snv 0.75
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 3 2008 2012
dbSNP: rs4970834
rs4970834 		0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2008 2012
dbSNP: rs611917
rs611917 		1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2008 2012
dbSNP: rs6657811
rs6657811 		1 109264661 intron variant A/C;T snv 4.0E-06; 0.10
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2008 2012
dbSNP: rs7528419
rs7528419 		0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs10858082
rs10858082 		1 109256099 intron variant G/A snv 0.48
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17035665
rs17035665 		1 109271097 intron variant C/T snv 0.19
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs3832016
rs3832016 		1 109275536 3 prime UTR variant -/T ins 0.74
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4970833
rs4970833 		1 109262024 intron variant G/A snv 0.36
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs57677983
rs57677983 		1 109275536 3 prime UTR variant C/A;G;T snv 1.1E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6689614
rs6689614 		1 109264477 synonymous variant G/A;C snv 0.44
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6698843
rs6698843 		0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012