rs6739779

This is a intergenic variant variant.

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

basal cell carcinoma

Allele T
OR
p 6.0e-77
N 307,684
Large GWAS
European
Liyanage UE et al. Combined analysis of keratinocyte cancers identifies novel genome-wide loci. Human Molecular Genetics 28(18):3148-3160 (2019)
Allele T
OR 1.15
p 7.0e-24
N 651,138
Large GWAS
European

keratinocyte carcinoma

Liyanage UE et al. Combined analysis of keratinocyte cancers identifies novel genome-wide loci. Human Molecular Genetics 28(18):3148-3160 (2019)
Allele C
OR 1.14
p 1.0e-19
N 358,840
Large GWAS
European

skin neoplasm

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele T
OR 0.13
p 2.0e-16
N 670,929
Large GWAS
multi-ancestry

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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