Original source

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

A/T | Ancestral: A | Ambiguity code: W

Chromosome 17:40819565 (forward strand) | View in location tab


with HGMD-PUBLIC CM941012 ; PhenCode HIFD_KRT10:c.1325T>A (A/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

Variation displays