rs17119461
This is a intergenic variant variant in the LINC02627 gene.
▶Research that mentions this SNP (1)
▶A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10qAssociationN=2,437Craig Teerlink et al.(2012)· Human Genetics
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q
AssociationN=2,437Craig Teerlink et al.(2012)· Human Genetics
A genome-wide association study in 156 melanoma cases from 34 high-risk Utah pedigrees identified three novel genome-wide significant SNPs on chromosome 10q25.1 (rs17119434, rs17119461, rs17119490) with p-values down to 7.21×10^-12 and odds ratios of 6.8-8.4, representing a unique approach to predisposition gene identification in related high-risk pedigrees.
Traits studied:Cutaneous malignant melanomaMelanoma susceptibility
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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