Original source

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

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

Chromosome 17:40822108 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941010, CM941009 ; 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 7 HGVS names - click the plus to show

Variation displays