Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_026_CYBA_608508_0005, 15771

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

Variation displays