Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome X:37796131 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980471, CM980470 ; PhenCode CYBBbase_D0025:g.17064C>A (C/A), CYBBbase_D0025:g.17064C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

This variation has 14 HGVS names - click the plus to show

Variation displays