Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)

Chromosome 5:132866989 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


ClinVar SCV000169720

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2543 sample genotypes and is associated with 1 phenotype.

Variant displays