Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.03 (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
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB KRT1:c.75C>T

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

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts, has 2813 sample genotypes and is associated with 1 phenotype.

Variant displays