Original source

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

Alleles
A/C/T|Ancestral: A|Ambiguity code: H
Location

Chromosome 14:36663232 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM013783

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_052_PAX9_167416_0002, 4523

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and is associated with 2 phenotypes.

Variant displays