Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 12:52488371 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT6A:c.1381G>A (C/T), HIFD_KRT6A:c.1381G>C (C/G)

Most severe consequence
Clinical significance

Synonyms

LSDB KRT6A:c.1381G>A, KRT6A:c.1381G>C

This variation has 6 HGVS names - click the plus to show

Variation displays