Original source

Variants (including SNPs and indels) imported from dbSNP (release 139)|View in dbSNP

Alleles
A/G|Ambiguity code: R
Location

Chromosome 5:45441639 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Synonyms

Archive dbSNP rs82439070

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays