Original source

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

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

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

Most severe consequence
Missense variant
Evidence status

Clinical significance


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