This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.01 (G)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB KRT12:c.*360A>C

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant has 2505 sample genotypes and is associated with 2 phenotypes.

Variant displays