Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/T|Ancestral: G|Ambiguity code: K

Chromosome 16:88643474 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM910096 ; PhenCode CYBAbase_D0024:g.8568C>A (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 2010_April_001_026_CYBA_608508_0005, 15771

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and is associated with 2 phenotypes.

Variant displays