rs16901995

This is a coding sequence variant variant in the LOC105374618 gene.

Research that mentions this SNP (1)

SNPs in LncRNA genes are associated with non‐small cell lung cancer in a Chinese population
AssociationN=3,023Ruoyang Wang et al.(2019)· Journal of Clinical Laboratory Analysis

A case-control study of 1,294 NSCLC cases and 1,729 healthy Chinese Han controls genotyped 17 SNPs in 13 lncRNA genes. Three SNPs showed significant associations with lung cancer risk: rs498238 (CC genotype OR=0.33, p=0.043), rs16901995 (CT/TT genotypes in non-smokers OR=0.78, p=0.035), and rs219741 (variant genotypes in young patients OR=1.47, p=0.033). No associations were found with overall survival.

Traits studied:Lung cancer riskNon-small cell lung cancer (NSCLC)Overall survival

This variant is in our database but has no known associations or PRS memberships yet.

Gene information from NCBI Gene. Variant classifications from ClinVar.

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