rs1805329, RAD23B

N. diseases: 15
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.020 0.500 2 2009 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.020 0.500 2 2009 2014
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2007 2007
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2013 2013
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2007 2007
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2009 2009
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2009 2009
Lymphoma, Follicular
CUI: C0024301
Disease: Lymphoma, Follicular
83 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2014 2014
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2013 2013
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2009 2009
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2007 2007
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2011 2011
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
82 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2007 2007
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2007 2007
Xeroderma pigmentosum, group A
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
55 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 0.010 1.000 1 2007 2007