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 12:53073570 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941001, CM994570 ; PhenCode HIFD_KRT1:c.563A>G (T/C), HIFD_KRT1:c.563A>C (T/G)

Most severe consequence

This variation has 3 synonyms - click the plus to show

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

Variation displays