Original source

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

Alleles
-/C
Location

Chromosome 11: between 5225720 and 5225721 (forward strand) | View in location tab

Co-located

with PhenCode HbVar.945 (-/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

HbVar 945

This variation has 4 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