SULT1A1, sulfotransferase family 1A member 1, 6817

N. diseases: 122; N. variants: 13
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: rs1336331763
rs1336331763
0.882 0.120 16 28606796 missense variant G/A snv 4.0E-06
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1432142550
rs1432142550
0.882 0.080 16 28606787 missense variant A/G snv 7.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1432142550
rs1432142550
0.882 0.080 16 28606787 missense variant A/G snv 7.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1432142550
rs1432142550
0.882 0.080 16 28606787 missense variant A/G snv 7.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung
Neoplasms; Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1801030
rs1801030
1.000 0.040 16 28606164 missense variant C/G;T snv 8.1E-06; 0.98
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2015 2015
dbSNP: rs767915085
rs767915085
0.882 0.080 16 28606122 missense variant T/C snv 8.0E-06 7.1E-06
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2005 2005
dbSNP: rs767915085
rs767915085
0.882 0.080 16 28606122 missense variant T/C snv 8.0E-06 7.1E-06
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs767915085
rs767915085
0.882 0.080 16 28606122 missense variant T/C snv 8.0E-06 7.1E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2005 2005
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0028754
Disease: Obesity
Obesity
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2004 2004
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2008 2008
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
Squamous cell carcinoma of the head and neck
Neoplasms 0.010 1.000 1 2006 2006
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
Digestive System Diseases; Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0238033
Disease: Carcinoma of Male Breast
Carcinoma of Male Breast
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2008 2008
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C2931456
Disease: Prostate cancer, familial
Prostate cancer, familial
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0017411
Disease: Female Genital Diseases
Female Genital Diseases
Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2006 2006
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C4054727
Disease: Infant Acute Lymphoblastic Leukemia
Infant Acute Lymphoblastic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0242787
Disease: Malignant neoplasm of male breast
Malignant neoplasm of male breast
Neoplasms; Skin and Connective Tissue Diseases; Endocrine System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial
Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
Environment-Related Malignant Neoplasm
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs9282861
rs9282861
0.658 0.440 16 28606193 missense variant C/T snv
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
Digestive System Diseases; Neoplasms 0.010 1.000 1 2004 2004