Original source

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

Alleles
T/A/G|Ancestral: T|Ambiguity code: D
Location

Chromosome 16:176721 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB HbVar.711, HbVar.1_1

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 20 transcripts, 2 regulatory features, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays