Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 13:20223371 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM020718

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 12670, 2010_April_001_053_GJB6_604418_0005

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays