Original source

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

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

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

Co-located

with HGMD-PUBLIC CM030695

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4526, 2010_April_001_054_PAX9_167416_0005

This variation has 7 HGVS names - click the plus to show

Variation displays