Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 5:150121956 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs62627086

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and 2 regulatory features.

Variant displays