Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.19 (A)
Location

Chromosome 12:52288357 (forward strand) | View in location tab

Co-located

with PhenCode HIFD_KRT81:c.735+4C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB KRT81:c.735+4C>T

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts, has 2510 individual genotypes and is associated with 1 phenotype.

Variation displays