XRCC5, X-ray repair cross complementing 5, 7520

N. diseases: 113; N. variants: 12
Disease: MYELODYSPLASTIC SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3835
rs3835
Entrez Id: 7520
Gene Symbol: XRCC5
XRCC5
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME 		0.010 GeneticVariation BEFREE We found that the A/G heterozygous genotype of the rs3835 polymorphism is associated with decreased chance of developing MDS (p < 0.001). 25312513 2015