Original source

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

Alleles
G/A|Ancestral: A|Ambiguity code: R|MAF: 0.34 (A)
Location

Chromosome 5:256357 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 6 synonyms - Show

HGVS names

This variant has 19 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, has 2510 sample genotypes and is associated with 2 phenotypes.

Variant displays