Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 13 HGVS names - click the plus to show

About this variant

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

Variant displays