CMA1, chymase 1, 1215

N. diseases: 157; N. variants: 2
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: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0017661
Disease: IGA Glomerulonephritis
IGA Glomerulonephritis
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases 0.020 1.000 2 2011 2011
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0019100
Disease: Severe Dengue
Severe Dengue
Infections 0.010 < 0.001 1 2015 2015
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0376300
Disease: Dengue Shock Syndrome
Dengue Shock Syndrome
Infections 0.010 1.000 1 2015 2015
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C1848296
Disease: DOSAGE-SENSITIVE SEX REVERSAL
DOSAGE-SENSITIVE SEX REVERSAL
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder)
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 < 0.001 1 2015 2015
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD
0.010 1.000 1 2011 2011
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease
0.010 1.000 1 2011 2011
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800875
rs1800875
0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41
CUI: C0013595
Disease: Eczema
Eczema
Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1800876
rs1800876
1.000 14 24510007 upstream gene variant G/A snv 0.24
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD
0.010 1.000 1 2011 2011
dbSNP: rs1800876
rs1800876
1.000 14 24510007 upstream gene variant G/A snv 0.24
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease
0.010 1.000 1 2011 2011