Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 16:176717 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM870011 ; PhenCode HbVar.1063 (A/G)

Most severe consequence
Evidence status

Synonyms

HbVar 1063

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

Variation displays