Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 16:88651007 (forward strand) | View in location tab

Co-located

with COSMIC COSM131493 (G/A) ; HGMD-PUBLIC CM001111 ; PhenCode CYBAbase_D0024:g.1035C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_029_CYBA_608508_0009, 15775

This variation has 15 HGVS names - click the plus to show

Variation displays