Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
AG/C
Location

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

Co-located variant

PhenCode HbVar.949 (AG/C)

Most severe consequence
 
Frameshift variant
Evidence status

Clinical significance

Synonyms

LSDB HbVar.949

HGVS names

This variant has 5 HGVS names - 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