Original source

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

A/C/G|Ancestral: A|Ambiguity code: V

Chromosome 12:52492669 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM015023 ; PhenCode HIFD_KRT6A:c.520T>G (A/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 6 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature and is associated with 4 phenotypes.

Variant displays