RAD51, RAD51 recombinase, 5888

N. diseases: 363; N. variants: 16
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555429623
rs1555429623
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C3281089
Disease:
MIRROR MOVEMENTS 2
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C4551570
Disease:
2-3 toe syndactyly
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0003466
Disease:
Anus, Imperforate
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0079924
Disease:
Oligohydramnios
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0557874
Disease:
Global developmental delay
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C1862102
Disease:
BRACHYDACTYLY, TYPE E1
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0423112
Disease:
Short palpebral fissure
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0221263
Disease:
Cafe-au-Lait Spots
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C1837404
Disease:
High, narrow palate
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C4284093
Disease:
FANCONI ANEMIA, COMPLEMENTATION GROUP R
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0345354
Disease:
Radial polydactyly
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0026827
Disease:
Muscle hypotonia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C1849020
Disease:
Short metatarsal
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C2673410
Disease:
Small midface
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0027092
Disease:
Myopia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0018817
Disease:
Atrial Septal Defects
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0009806
Disease:
Constipation
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C1855222
Disease:
Delayed proximal femoral epiphyseal ossification
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C1837731
Disease:
Overfolded helix
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0005745
Disease:
Blepharoptosis
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0349588
Disease:
Short stature
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C1850049
Disease:
Clinodactyly of the 5th finger
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C4551563
Disease:
Microcephaly (physical finding)
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555429629
rs1555429629
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0235752
Disease:
Port-Wine Stain
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1801320
rs1801320
Entrez Id: 5888;100505648
Gene Symbol: RAD51;RAD51-AS1
RAD51;RAD51-AS1
CUI: C4016360
Disease:
BREAST CANCER, SUSCEPTIBILITY TO, IN BRCA1 AND BRCA2 CARRIERS
C 0.700 SusceptibilityMutation CLINVAR