Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 14:23898214 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM087715, CM920490 ; PhenCode FHC0121 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 29168, 4195

This variation has 12 HGVS names - click the plus to show

Variation displays