Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1950897
rs1950897
RAD51B
0.925 0.160 14 68293424 intron variant C/G;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.800 1.000 2 2014 2019
dbSNP: rs4902632
rs4902632
RAD51B
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
RAD51B
1.000 0.080 14 68276590 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs11158717
rs11158717
RAD51B
14 68047559 intron variant A/G;T snv
CUI: C0018498
Disease: Hair Color
Hair Color 		0.700 1.000 1 2018 2018
dbSNP: rs11629144
rs11629144
RAD51B
14 68664876 intron variant G/A;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1290999
rs1290999
RAD51B
1.000 0.040 14 68579159 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs140825531
rs140825531
RAD51B
1.000 0.120 14 68021957 intron variant G/A;C snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.700 1.000 1 2018 2018
dbSNP: rs1950897
rs1950897
RAD51B
0.925 0.160 14 68293424 intron variant C/G;T snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs1950897
rs1950897
RAD51B
0.925 0.160 14 68293424 intron variant C/G;T snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2025009
rs2025009
RAD51B ; LOC107984679
1.000 0.080 14 68376888 intron variant G/A;C snv
CUI: C4277682
Disease: Chemical and Drug Induced Liver Injury
Chemical and Drug Induced Liver Injury 		0.700 1.000 1 2017 2017
dbSNP: rs35190649
rs35190649
RAD51B
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: rs4902562
rs4902562
RAD51B
1.000 0.080 14 68264741 intron variant A/G;T snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs56267624
rs56267624
RAD51B
1.000 0.080 14 68195642 intron variant C/T snv 3.9E-02
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2018 2018
dbSNP: rs56267624
rs56267624
RAD51B
1.000 0.080 14 68195642 intron variant C/T snv 3.9E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2018 2018
dbSNP: rs10138752
rs10138752
RAD51B
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: rs10138752
rs10138752
RAD51B
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
RAD51B
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
RAD51B
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
RAD51B
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: rs4902602
rs4902602
RAD51B
1.000 0.040 14 68574615 intron variant A/G snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs72725119
rs72725119
RAD51B
14 67862303 intron variant G/A snv 0.12
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs1314913
rs1314913
RAD51B
0.807 0.120 14 68232877 intron variant C/T snv 0.13
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.830 1.000 1 2012 2019
dbSNP: rs4902592
rs4902592
RAD51B
14 68455304 intron variant T/C snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs72725174
rs72725174
RAD51B
14 68044056 intron variant C/T snv 0.13
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs11158743
rs11158743
RAD51B
14 68439257 intron variant C/T snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019