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

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

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

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB HbVar.567_1, HbVar.567, 30135

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