Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome X:37799011 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910101, CM950329 ; PhenCode CYBBbase_D0025:g.19944G>A (G/A), CYBBbase_D0025:g.19944G>C (G/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, is associated with 5 phenotypes and is mentioned in 2 citations.

Variant displays