ALB, albumin, 213

N. diseases: 1198; N. variants: 21
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: rs77892378
rs77892378 		1.000 0.080 4 73406760 missense variant T/C;G snv
CUI: C0342185
Disease: Hyperthyroxinemia, Familial Dysalbuminemic
Hyperthyroxinemia, Familial Dysalbuminemic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases 0.800 1.000 4 1994 1998
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.020 1.000 2 2007 2009
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.020 1.000 2 2007 2009
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 0.500 2 2006 2013
dbSNP: rs11538209
rs11538209 		1.000 0.120 4 73404356 missense variant T/C snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs11538209
rs11538209 		1.000 0.120 4 73404356 missense variant T/C snv
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 < 0.001 1 2001 2001
dbSNP: rs1162592300
rs1162592300 		0.925 0.080 4 73412045 missense variant G/A snv
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2003 2003
dbSNP: rs1162592300
rs1162592300 		0.925 0.080 4 73412045 missense variant G/A snv
CUI: C0243050
Disease: Cardiovascular Abnormalities
Cardiovascular Abnormalities 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases 0.010 1.000 1 2003 2003
dbSNP: rs1162592300
rs1162592300 		0.925 0.080 4 73412045 missense variant G/A snv
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2003 2003
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs1332629192
rs1332629192 		0.851 0.200 4 73404374 missense variant C/T snv
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs374651285
rs374651285 		4 73406645 missense variant G/A snv
CUI: C0027765
Disease: nervous system disorder
nervous system disorder 		Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs75353611
rs75353611 		4 73404401 missense variant A/T snv
CUI: C3889611
Disease: ALBUMIN BLENHEIM PHENOTYPE
ALBUMIN BLENHEIM PHENOTYPE 		0.700 0
dbSNP: rs77335374
rs77335374 		4 73411994 splice acceptor variant A/G;T snv
CUI: C0878666
Disease: Analbuminemia
Analbuminemia 		0.700 0
dbSNP: rs77449454
rs77449454 		4 73413444 frameshift variant -/A delins
CUI: C0878666
Disease: Analbuminemia
Analbuminemia 		0.700 0
dbSNP: rs79228041
rs79228041 		4 73419634 missense variant G/A snv
CUI: C4015752
Disease: ALBUMIN B PHENOTYPE
ALBUMIN B PHENOTYPE 		0.700 0
dbSNP: rs77238412
rs77238412 		4 73408735 stop gained C/G;T snv 4.0E-06
CUI: C0878666
Disease: Analbuminemia
Analbuminemia 		0.700 1.000 3 1994 2005
dbSNP: rs1171303257
rs1171303257 		4 73410405 missense variant G/C snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 1998 1998
dbSNP: rs1171303257
rs1171303257 		4 73410405 missense variant G/C snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 1998 1998
dbSNP: rs1241977606
rs1241977606 		0.925 0.080 4 73416326 missense variant A/G snv 4.0E-06
CUI: C3874381
Disease: Childhood nephrotic syndrome
Childhood nephrotic syndrome 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2006 2006
dbSNP: rs1241977606
rs1241977606 		0.925 0.080 4 73416326 missense variant A/G snv 4.0E-06
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2006 2006
dbSNP: rs762334560
rs762334560 		1.000 0.080 4 73404391 missense variant T/C snv 8.0E-06 7.0E-06
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs74821926
rs74821926 		1.000 0.160 4 73404398 missense variant G/A;C;T snv 1.2E-05; 8.0E-06
CUI: C4551623
Disease: EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases 0.700 0