Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 12:52952163 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT18:c.993C>T (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB KRT18:c.993C>T

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts, 2 regulatory features and is associated with 1 phenotype.

Variant displays