Original source

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

T/G | Ancestral: T | Ambiguity code: K

Chromosome 17:38978378 (forward strand) | View in location tab


with HGMD-PUBLIC CM941006 ; PhenCode HIFD_KRT10:c.460A>C (T/G)

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