Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome X:37803890 (forward strand) | View in location tab


with HGMD-PUBLIC CM015924, CM106190 ; PhenCode CYBBbase_D0025:g.24827C>G (C/G), CYBBbase_D0025:g.24827C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

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

About this variant

This variant overlaps 4 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variation displays