LIPC, lipase C, hepatic type, 3990

N. diseases: 120; N. variants: 95
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: rs2070895
rs2070895 		0.807 0.120 15 58431740 intron variant G/A snv 0.33
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 3 2012 2012
dbSNP: rs1077834
rs1077834 		15 58431280 intron variant T/C snv 0.34
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2018 2019
dbSNP: rs1077834
rs1077834 		15 58431280 intron variant T/C snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2017 2018
dbSNP: rs1800588
rs1800588 		0.790 0.200 15 58431476 intron variant C/G;T snv 0.30
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2008 2012
dbSNP: rs261334
rs261334 		15 58434545 intron variant G/C snv 0.73
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs261342
rs261342 		15 58438954 intron variant G/A;C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs473224
rs473224 		15 58445142 intron variant T/A;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2009 2012
dbSNP: rs588136
rs588136 		15 58438299 intron variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2012 2013
dbSNP: rs8034802
rs8034802 		15 58432593 intron variant T/A snv 0.33
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2012 2012
dbSNP: rs10152202
rs10152202 		15 58452149 intron variant T/G snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10518976
rs10518976 		15 58459002 intron variant T/A snv 7.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10518982
rs10518982 		15 58507555 intron variant A/G snv 2.2E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10518982
rs10518982 		15 58507555 intron variant A/G snv 2.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10518982
rs10518982 		15 58507555 intron variant A/G snv 2.2E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10518983
rs10518983 		15 58520578 intron variant C/T snv 5.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1077834
rs1077834 		15 58431280 intron variant T/C snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1077834
rs1077834 		15 58431280 intron variant T/C snv 0.34
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1077835
rs1077835 		15 58431227 intron variant A/G snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1077835
rs1077835 		15 58431227 intron variant A/G snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1077835
rs1077835 		15 58431227 intron variant A/G snv 0.34
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2013 2013
dbSNP: rs11071380
rs11071380 		15 58418428 intron variant C/A snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11071381
rs11071381 		15 58429415 intron variant G/A snv 0.36
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11631342
rs11631342 		1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.700 1.000 1 2018 2018
dbSNP: rs11632618
rs11632618 		15 58432507 intron variant G/A;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11632618
rs11632618 		15 58432507 intron variant G/A;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012