Original source

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

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

Chromosome 16:88713169 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15772, 2010_April_001_027_CYBA_608508_0006

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

Variation displays