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: 0.01 (G)
Location

Chromosome 5:132294361 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs567027433

HGVS names

This variant has 6 HGVS names - Show

About this variant

Variant displays