Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 16:88646773 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM101776, CM920219 ; PhenCode CYBAbase_D0024:g.5269G>A (C/T), CYBAbase_D0024:g.5269G>C (C/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15769, 2010_April_001_024_CYBA_608508_0003

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

Variation displays