Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768043782
rs768043782
Entrez Id: 1030;100048912
Gene Symbol: CDKN2B;CDKN2B-AS1
CDKN2B;CDKN2B-AS1
CUI: C3811653
Disease:
Experimental Organism Basal Cell Carcinoma
0.010 GeneticVariation BEFREE SNP rs11170164, encoding a G138E substitution in the keratin 5 (KRT5) gene, affects risk of BCC (OR = 1.35, P = 2.1 x 10(-9)). 19578363 2009