Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)

Chromosome 6:1610850 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


ClinVar SCV000202732

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 2598 sample genotypes and is associated with 1 phenotype.

Variant displays