Original source

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

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

Chromosome 14:37132173 (forward strand) | View in location tab

Co-located

with COSMIC COSM39639 (C/T) ; HGMD-PUBLIC CM032984

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_056_PAX9_167416_0008, 4529

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

Variation displays