LIPG, lipase G, endothelial type, 9388

N. diseases: 62; N. variants: 18
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: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 3 2014 2018
dbSNP: rs12970066
rs12970066 		18 49580782 intron variant C/A;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2016 2018
dbSNP: rs149615216
rs149615216 		18 49579658 intron variant C/T snv 5.6E-03
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 2 2017 2018
dbSNP: rs149615216
rs149615216 		18 49579658 intron variant C/T snv 5.6E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2018 2018
dbSNP: rs11082764
rs11082764 		18 49593209 3 prime UTR variant A/G snv 0.13
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11875600
rs11875600 		18 49572816 intron variant A/G snv 0.12
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11875600
rs11875600 		18 49572816 intron variant A/G snv 0.12
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12966382
rs12966382 		18 49559070 upstream gene variant C/T snv 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs12966382
rs12966382 		18 49559070 upstream gene variant C/T snv 0.11
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2000813
rs2000813 		0.763 0.200 18 49567494 missense variant C/A;T snv 4.0E-06; 0.27; 4.0E-06 0.23
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		Mental Disorders 0.700 1.000 1 2012 2012
dbSNP: rs201922257
rs201922257 		18 49569492 missense variant C/T snv 1.7E-04 2.7E-04
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2017 2017
dbSNP: rs201922257
rs201922257 		18 49569492 missense variant C/T snv 1.7E-04 2.7E-04
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs35816125
rs35816125 		1.000 0.080 18 49562460 intron variant C/G snv 0.25
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2019 2019
dbSNP: rs35816125
rs35816125 		1.000 0.080 18 49562460 intron variant C/G snv 0.25
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs3786247
rs3786247 		18 49592553 3 prime UTR variant T/G snv 0.13
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017
dbSNP: rs3786247
rs3786247 		18 49592553 3 prime UTR variant T/G snv 0.13
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4245232
rs4245232 		18 49560628 upstream gene variant A/C;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4245232
rs4245232 		18 49560628 upstream gene variant A/C;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs77960347
rs77960347 		18 49583585 missense variant A/C;G snv 4.0E-06; 8.7E-03
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs8093249
rs8093249 		18 49571028 intron variant A/G snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs8093249
rs8093249 		18 49571028 intron variant A/G snv 0.14
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs874565
rs874565 		18 49562320 synonymous variant C/A;T snv 9.4E-03
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012