Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)

Chromosome 21:36461009 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts, has 2857 sample genotypes, is associated with 2 phenotypes and is mentioned in 6 citations.

Variant displays