Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.33 (C)

Chromosome 16:28887472 (forward strand) | View in location tab


with COSMIC COSM3754834 (T/C)

Most severe consequence
Evidence status

Clinical significance


This variation has 4 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2326 individual genotypes and is associated with 2 phenotypes.

Variation displays