Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome X:18581942 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042955 ; PhenCode RettBASE_CDKL5:c.455G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Variation displays