Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_052_PAX9_167416_0002, 4523

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

Variation displays