Variant (rsID / SNP)

rs1023065

rs1023065 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CASK. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CASKLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Cytoband: Xp11.4
HGVS: NM_001367721.1(CASK):c.429+11419A>G
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.