Original source

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

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

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


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

About this variant

This variant overlaps 3 transcripts, is associated with 3 phenotypes and is mentioned in 4 citations.

Variation displays