Original source

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

Alleles
CCGCGC/-|MAF: 0.36 (CCGCGC)
Location

Chromosome 5:135028717-135028722 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs145747214

HGVS names

This variant has 3 HGVS names - Show

About this variant

Variant displays