This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C/T | Ancestral: G | Ambiguity code: B | MAF: < 0.01 (C)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB KRT12:c.55C>T

HGVS name

None

About this variant

This variant has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays