Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H
Location

Chromosome 11:5225486 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR900266, CR057232 ; PhenCode HbVar.970 (T/C), HbVar.2720 (T/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

HbVar 970, 2720

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays