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: rs2189517
rs2189517
0.882 0.080 14 68536271 intron variant A/G snv 0.49
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs2189517
rs2189517
0.882 0.080 14 68536271 intron variant A/G snv 0.49
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2020 2020
dbSNP: rs2189517
rs2189517
0.882 0.080 14 68536271 intron variant A/G snv 0.49
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.010 1.000 1 2020 2020
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: rs10483813
rs10483813
0.851 0.120 14 68564567 intron variant T/A;C snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.030 0.667 3 2010 2019
dbSNP: rs10483813
rs10483813
0.851 0.120 14 68564567 intron variant T/A;C snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
Neoplasms; Skin and Connective Tissue Diseases 0.030 0.667 3 2010 2019
dbSNP: rs1314913
rs1314913
0.807 0.120 14 68232877 intron variant C/T snv 0.13
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
Neoplasms; Skin and Connective Tissue Diseases 0.030 1.000 3 2015 2019
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: 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: 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: 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: 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: 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: 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: rs1885013
rs1885013
0.925 0.080 14 68287978 intron variant G/A snv 0.57
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1885013
rs1885013
0.925 0.080 14 68287978 intron variant G/A snv 0.57
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1950897
rs1950897
0.925 0.160 14 68293424 intron variant C/G;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1950897
rs1950897
0.925 0.160 14 68293424 intron variant C/G;T snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
Respiratory Tract Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2588809
rs2588809
0.807 0.160 14 68193711 intron variant T/C snv 0.80
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs28649231
rs28649231
14 67956498 intron variant G/A snv 0.18
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs35190649
rs35190649
14 68410812 intron variant T/C;G snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs3784099
rs3784099
0.807 0.320 14 68283210 intron variant G/A snv 0.43
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs4902592
rs4902592
14 68455304 intron variant T/C snv 0.13
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019