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 14:56802340 (forward strand) | View in location tab

Co-located

with COSMIC COSM257656 (G/A) ; HGMD-PUBLIC CM104945, CM051593

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_049_OTX2_600037_0002, 8841

This variation has 13 HGVS names - click the plus to show

Variation displays