This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T|Ancestral: C|Ambiguity code: N
Location

Chromosome 11:5225607 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB HbVar.567_1, 30135, HbVar.567

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 3 citations.

Variant displays