Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome X:153791828 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074908 ; PhenCode IKBKGbase_D0046:g.21349G>C (G/C)

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_042666

This variation has 25 HGVS names - click the plus to show

Variation displays