Original source

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

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

Chromosome X:154561696 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM011369 ; PhenCode IKBKGbase_D0046:g.19432T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_011321

This variation has 24 HGVS names - click the plus to show

Variation displays