Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 11:5246716 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

HbVar 2720, 970

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

Variation displays