Original source

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

Alleles
TTATT/-
Location

Chromosome 11:5225486-5225490 (forward strand) | View in location tab

Co-located

with PhenCode HbVar.973 (TTATT/-)

Most severe consequence
Evidence status

Clinical significance

Synonyms

HbVar 973

This variation has 2 HGVS names - click the plus to show

Variation displays