Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.34 (A)
Location

Chromosome X:18579749 (forward strand) | View in location tab

Co-located

with PhenCode RettBASE_CDKL5:c.283-99C>A (C/A)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays