Original source

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

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

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

Co-located variants

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

Most severe consequence
Start lost
Evidence status


LSDB HbVar.1063

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 2 regulatory features, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays