RAD51, RAD51 recombinase, 5888

N. diseases: 363; N. variants: 16
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: rs11855560
rs11855560 		15 40732105 3 prime UTR variant T/C snv 0.49
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs1247974770
rs1247974770 		15 40718820 missense variant G/T snv 8.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1247974770
rs1247974770 		15 40718820 missense variant G/T snv 8.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs752492487
rs752492487 		15 40718847 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.020 1.000 2 2016 2018
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2007 2011
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		Neoplasms 0.020 1.000 2 2016 2018
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.020 1.000 2 2007 2011
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0278878
Disease: Adult Glioblastoma
Adult Glioblastoma 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2014 2014
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		Neoplasms; Female Urogenital Diseases and Pregnancy Complications 0.010 1.000 1 2014 2014
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		Hemic and Lymphatic Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C0280474
Disease: Childhood Glioblastoma
Childhood Glioblastoma 		Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs1801320
rs1801320 		0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12
CUI: C4016360
Disease: BREAST CANCER, SUSCEPTIBILITY TO, IN BRCA1 AND BRCA2 CARRIERS
BREAST CANCER, SUSCEPTIBILITY TO, IN BRCA1 AND BRCA2 CARRIERS 		0.700 0
dbSNP: rs1555429629
rs1555429629 		0.763 0.200 15 40729632 missense variant G/A snv
CUI: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly 		0.700 0
dbSNP: rs1555429629
rs1555429629 		0.763 0.200 15 40729632 missense variant G/A snv
CUI: C0235752
Disease: Port-Wine Stain
Port-Wine Stain 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs1555429629
rs1555429629 		0.763 0.200 15 40729632 missense variant G/A snv
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.700 0
dbSNP: rs1555429629
rs1555429629 		0.763 0.200 15 40729632 missense variant G/A snv
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases 0.700 0
dbSNP: rs1555429629
rs1555429629 		0.763 0.200 15 40729632 missense variant G/A snv
CUI: C1837404
Disease: High, narrow palate
High, narrow palate 		0.700 0
dbSNP: rs1555429629
rs1555429629 		0.763 0.200 15 40729632 missense variant G/A snv
CUI: C1849020
Disease: Short metatarsal
Short metatarsal 		0.700 0