Original source

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

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

Chromosome 14:37132248 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033976

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4534, 2010_April_001_058_PAX9_167416_0013

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

Variation displays