Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 12:52680274 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT1:c.75C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB KRT1:c.75C>T

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays