Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 14:36662975 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040239

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4528, 2010_April_001_055_PAX9_167416_0007

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

Variation displays