Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.20 (A)
Location

Chromosome 3:49664550 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs56540553, rs57210211

HGVS names

This variant has 3 HGVS names - Hide

3:g.49664550G>A
ENST00000296452.4:c.11736G>A
ENST00000296452.4:c.11736G>A(p.=)

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 transcripts, has 4071 sample genotypes, is associated with 4 phenotypes and is mentioned in 43 citations.

Variant displays