Original source

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

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

Chromosome 12:52885522 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT6A:c.541-2A>C (T/G), HIFD_KRT6A:c.541-2A>G (T/C)

Most severe consequence
Synonyms

LSDB KRT6A:c.541-2A>G, KRT6A:c.541-2A>C

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

Variation displays