Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 17:40822210 (forward strand) | View in location tab

Co-located

with COSMIC COSM1128722 (C/T) ; PhenCode HIFD_KRT10:c.376G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

This variation has assays on 5 chips - click the plus to show

Variation displays