Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome X:154556314 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM045871 ; PhenCode IKBKGbase_D0046:g.14049G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_026493

This variation has 31 HGVS names - click the plus to show

Variation displays