Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome X:37810805 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980491 ; PhenCode CYBBbase_D0025:g.31742T>A (T/A)

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

Variation displays