Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 17:38978360 (forward strand) | View in location tab


with HGMD-PUBLIC CM941009, CM941010 ; PhenCode HIFD_KRT10:c.478T>G (A/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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

Variation displays