Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:37796092 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD011999, CM910100 ; PhenCode CYBBbase_D0025:g.17025C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variation displays