Original source

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

Alleles
CCT/-
Location

Chromosome 11:5225657-5225659 (forward strand)|View in location tab

Co-located variant

PhenCode HbVar.962 (CCT/-)

Most severe consequence
 
Inframe deletion
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays