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: rs1314913
rs1314913
0.807 0.120 14 68232877 intron variant C/T snv 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.830 1.000 4 2012 2019
dbSNP: rs8017304
rs8017304
1.000 0.040 14 68318360 intron variant G/A snv 0.54
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.830 1.000 4 2013 2019
dbSNP: rs2588809
rs2588809
0.807 0.160 14 68193711 intron variant T/C snv 0.80
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.820 1.000 6 2012 2017
dbSNP: rs911263
rs911263
0.851 0.200 14 68286876 intron variant C/T snv 0.57
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
Pathological Conditions, Signs and Symptoms; Digestive System Diseases 0.800 1.000 3 2011 2015
dbSNP: rs1744947
rs1744947
1.000 0.080 14 68214759 intron variant C/T snv 0.18
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.800 1.000 2 2012 2017
dbSNP: rs1950897
rs1950897
0.925 0.160 14 68293424 intron variant C/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.800 1.000 2 2014 2019
dbSNP: rs8022206
rs8022206
14 68054189 intron variant G/A snv 0.18
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.800 1.000 1 2011 2011
dbSNP: rs999737
rs999737
0.776 0.200 14 68567965 intron variant C/T snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.770 0.909 11 2009 2017
dbSNP: rs999737
rs999737
0.776 0.200 14 68567965 intron variant C/T snv 0.16
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.770 0.889 9 2009 2016
dbSNP: rs2588809
rs2588809
0.807 0.160 14 68193711 intron variant T/C snv 0.80
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.720 1.000 3 2013 2016
dbSNP: rs911263
rs911263
0.851 0.200 14 68286876 intron variant C/T snv 0.57
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.720 1.000 3 2013 2017
dbSNP: rs4902632
rs4902632
14 68682711 intron variant A/C;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 2 2018 2019
dbSNP: rs7141529
rs7141529
0.925 0.080 14 68660027 intron variant T/C snv 0.53
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.700 1.000 2 2013 2018
dbSNP: rs10131490
rs10131490
1.000 0.080 14 68276590 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs10138752
rs10138752
14 68713254 intron variant C/T snv 8.8E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10138752
rs10138752
14 68713254 intron variant C/T snv 8.8E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs10138752
rs10138752
14 68713254 intron variant C/T snv 8.8E-02
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1.000 1 2016 2016
dbSNP: rs10138752
rs10138752
14 68713254 intron variant C/T snv 8.8E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2016 2016
dbSNP: rs10138752
rs10138752
14 68713254 intron variant C/T snv 8.8E-02
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs1028842
rs1028842
1.000 0.080 14 68205006 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: rs11158716
rs11158716
14 68026441 intron variant G/A snv 0.17
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs11158716
rs11158716
14 68026441 intron variant G/A snv 0.17
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs11158717
rs11158717
14 68047559 intron variant A/G;T snv
CUI: C0018498
Disease: Hair Color
Hair Color
0.700 1.000 1 2018 2018
dbSNP: rs11158743
rs11158743
14 68439257 intron variant C/T snv 0.13
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs11624333
rs11624333
1.000 0.080 14 68513118 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 2017 2017