Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs714052
rs714052
BAZ1B
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 3 2009 2019
dbSNP: rs1178979
rs1178979
BAZ1B
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
BAZ1B
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: rs1178979
rs1178979
BAZ1B
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 1 2010 2017
dbSNP: rs1178979
rs1178979
BAZ1B
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 1 2010 2017
dbSNP: rs17145713
rs17145713
BAZ1B
0.925 0.120 7 73490480 intron variant C/T snv 0.21
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		0.800 1.000 1 2010 2010
dbSNP: rs17145713
rs17145713
BAZ1B
0.925 0.120 7 73490480 intron variant C/T snv 0.21
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		0.800 1.000 1 2010 2010
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2012 2016
dbSNP: rs1178977
rs1178977
BAZ1B
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: rs13231516
rs13231516
BAZ1B
7 73448919 intron variant T/C;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2016 2019
dbSNP: rs1178977
rs1178977
BAZ1B
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
dbSNP: rs13244268
rs13244268
BAZ1B
0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs13244268
rs13244268
BAZ1B
0.925 0.120 7 73497513 intron variant T/C snv 9.2E-02
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs200548390
rs200548390
BAZ1B
1.000 0.040 7 73478187 missense variant T/C snv 3.3E-04 3.5E-05
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia 		0.700 1.000 1 2018 2018
dbSNP: rs202203062
rs202203062
BAZ1B
7 73443388 intron variant G/- del
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia 		0.700 1.000 1 2017 2017
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2074755
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016