Original source

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

C/A | Ancestral: C | Ambiguity code: M

Chromosome X:37803886 (forward strand) | View in location tab


with HGMD-PUBLIC CP025134, CM015931 ; PhenCode CYBBbase_D0025:g.24823C>A (C/A), CYBBbase_D0025:g.24823C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Variation displays