Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 16:88643474 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910096 ; PhenCode CYBAbase_D0024:g.8568C>A (G/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_026_CYBA_608508_0005, 15771

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and is associated with 2 phenotypes.

Variant displays