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

Co-located

with HGMD-PUBLIC CM013783

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_052_PAX9_167416_0002, 4523

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays