Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 16:176752 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB HbVar.14_3, HbVar.14_1

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays