RAD51B, RAD51 paralog B, 5890

N. diseases: 126; N. variants: 108
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: rs116264287
rs116264287
1.000 0.080 14 68221985 intron variant C/T snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11629144
rs11629144
14 68664876 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs117351774
rs117351774
1.000 0.080 14 68221922 intron variant T/C snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
Malignant neoplasm of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C1335177
Disease: Ovarian Serous Adenocarcinoma
Ovarian Serous Adenocarcinoma
Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0346163
Disease: Endometrioid carcinoma ovary
Endometrioid carcinoma ovary
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0919267
Disease: ovarian neoplasm
ovarian neoplasm
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C1319315
Disease: Adenocarcinoma of large intestine
Adenocarcinoma of large intestine
Digestive System Diseases; Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
CUI: C0149782
Disease: Squamous cell carcinoma of lung
Squamous cell carcinoma of lung
Neoplasms; Respiratory Tract Diseases 0.700 1.000 1 2016 2016
dbSNP: rs11844632
rs11844632
0.708 0.280 14 68559662 intron variant G/A snv 0.23
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
0.700 1.000 1 2016 2016
dbSNP: rs12435046
rs12435046
14 68406810 intron variant T/G snv 0.44
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs1274638
rs1274638
1.000 0.080 14 68200005 intron variant T/C snv 0.15
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1274639
rs1274639
1.000 0.080 14 68201782 intron variant C/A snv 0.17
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1274640
rs1274640
1.000 0.080 14 68201811 intron variant C/T snv 0.15
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1274642
rs1274642
1.000 0.080 14 68205986 intron variant G/A snv 0.17
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012