Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B|MAF: 0.02 (G)
Location

Chromosome 14:22551882 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60541068

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays