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: rs13231516
rs13231516 		7 73448919 intron variant T/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2016 2019
dbSNP: rs10239940
rs10239940 		7 73487060 intron variant A/T snv 2.6E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10239940
rs10239940 		7 73487060 intron variant A/T snv 2.6E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1306476
rs1306476 		7 73454192 intron variant A/G snv 0.23
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13221253
rs13221253 		7 73507903 intron variant A/G snv 0.13
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs13231516
rs13231516 		7 73448919 intron variant T/C;G snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs202203062
rs202203062 		7 73443388 intron variant G/- del
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs34763247
rs34763247 		7 73452286 intron variant A/T snv 9.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35330527
rs35330527 		7 73455877 intron variant A/G snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35695283
rs35695283 		7 73479073 intron variant A/G snv 9.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs35797675
rs35797675 		7 73463714 intron variant T/G snv 0.20
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs62465144
rs62465144 		7 73468776 intron variant T/C snv 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7797566
rs7797566 		7 73482065 intron variant A/C snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs200548390
rs200548390 		1.000 0.040 7 73478187 missense variant T/C snv 3.3E-04 3.5E-05
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs714052
rs714052 		0.925 0.120 7 73450539 intron variant A/G snv 9.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 5 2009 2019
dbSNP: rs1178977
rs1178977 		0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		0.700 1.000 2 2013 2019
dbSNP: rs1178979
rs1178979 		0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.800 1.000 2 2010 2017
dbSNP: rs1178979
rs1178979 		0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.800 1.000 2 2010 2017
dbSNP: rs1178979
rs1178979 		0.925 0.120 7 73442100 3 prime UTR variant T/C snv 0.21
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2010 2019
dbSNP: rs2240466
rs2240466 		0.925 0.120 7 73441939 3 prime UTR variant G/A snv 9.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2009 2019
dbSNP: rs1178977
rs1178977 		0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.700 1.000 1 2010 2010
dbSNP: rs1178977
rs1178977 		0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs1178977
rs1178977 		0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal Diseases 0.700 1.000 1 2013 2013
dbSNP: rs1178977
rs1178977 		0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1178977
rs1178977 		0.925 0.120 7 73442719 splice region variant A/G snv 0.16 0.21
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2017 2017