Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.38 (A)
Location

Chromosome 11:71435531 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3184254

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 8 transcripts, has 2543 sample genotypes and is associated with 1 phenotype.

Variant displays