Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 14:36662954 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM030695

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4526, 2010_April_001_054_PAX9_167416_0005

HGVS names

This variant has 7 HGVS names - Show

About this variant

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

Variant displays