Original source

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

Alleles
C/A/G | Ancestral: C | Ambiguity code: V
Location

Chromosome 12:52491737 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT6A:c.541-1G>C (C/G), HIFD_KRT6A:c.541-1G>T (C/A)

Most severe consequence
Clinical significance

Synonyms

LSDB KRT6A:c.541-1G>C, KRT6A:c.541-1G>T

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

Variation displays