Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 14:36663163 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030696

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4525, 2010_April_001_053_PAX9_167416_0004

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

Variation displays