Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 16:88646761 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920220 ; PhenCode CYBAbase_D0024:g.5281A>G (T/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_027_CYBA_608508_0006, 15772

This variant has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and is associated with 2 phenotypes.

Variant displays