Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
CCT/-
Location

Chromosome 11:5225657-5225659 (forward strand) | View in location tab

Co-located

with PhenCode HbVar.962 (CCT/-)

Most severe consequence
Evidence status

Clinical significance

Synonyms

HbVar 962

This variation has 4 HGVS names - click the plus to show

Variation displays