Original source

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

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

Chromosome 21:36461442 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM011286

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_004_CLDN14_605608_0002, 13320

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and is associated with 2 phenotypes.

Variant displays