Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.22 (T)

Chromosome 3:58430808 (forward strand) | View in location tab


with COSMIC COSM3760211 (C/T), COSM1047802 (C/A)

Most severe consequence
Evidence status

Clinical significance


This variation has 9 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 15 transcripts, has 1107 individual genotypes and is associated with 1 phenotype.

Variation displays