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 12:21178955 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.10:g.21223156T>A

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts.

Variant displays