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

About this variant

This variant overlaps 6 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays