Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

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

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant 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.

Variant displays