Original source

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

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

Chromosome 12:52315936 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050656 ; PhenCode HIFD_KRT83:c.1219G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11443, KRT83:c.1219G>A

This variation has 3 HGVS names - click the plus to show

Variation displays