Original source

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

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

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

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


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