Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.15 (T)

Chromosome 2:232545584 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 6 transcripts, has 3863 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays