Original source

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

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

Chromosome X:154558649 (forward strand) | View in location tab


with HGMD-PUBLIC CM062780 ; PhenCode IKBKGbase_D0046:g.16384C>G (C/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

Variation displays