NBN, nibrin, 4683

N. diseases: 291; N. variants: 194
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2735383
rs2735383
Entrez Id: 734;4683
Gene Symbol: OSGIN2;NBN
OSGIN2;NBN
CUI: C0595989
Disease:
Carcinoma of larynx
0.010 GeneticVariation BEFREE NBS1 rs2735383 polymorphism is associated with an increased risk of laryngeal carcinoma. 29433451 2018