Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
 
Frameshift variant
Evidence status

Clinical significance

Synonyms

HbVar 945

This variant has 5 HGVS names - click the plus to show

About this variant

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

Variant displays