Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
AG/C
Location

Chromosome 11:5225698-5225699 (forward strand) | View in location tab

Co-located

with PhenCode HbVar.949 (AG/C)

Most severe consequence
 
Frameshift variant
Evidence status

Clinical significance

Synonyms

HbVar 949

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 2 phenotypes and is mentioned in 1 citation.

Variant displays