Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 17:40822137 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941005, CM941004 ; PhenCode HIFD_KRT10:c.449T>G (A/C), HIFD_KRT10:c.449T>C (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variation displays