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: rs9282861
rs9282861 		0.658 0.440 16 28606193 missense variant C/T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.020 1.000 2 2004 2004
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2004 2004
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
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: 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: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2004 2004
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 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: 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: 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: 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: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0017411
Disease: Female Genital Diseases
Female Genital Diseases 		Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2006 2006
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
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: C1168401
Disease: Squamous cell carcinoma of the head and neck
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: C0017411
Disease: Female Genital Diseases
Female Genital Diseases 		Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2006 2006
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2008 2008
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
CUI: C2931456
Disease: Prostate cancer, familial
Prostate cancer, familial 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
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: rs1182154114
rs1182154114 		0.925 0.080 16 28623160 missense variant G/C 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: rs1182154114
rs1182154114 		0.925 0.080 16 28623160 missense variant G/C 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: 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
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: rs1042028
rs1042028 		0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30
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: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2010 2010