Variant (rsID / SNP)

rs11718593

rs11718593 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARL13B. Location: chromosome 3, position 93,715,030. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ARL13BLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:93715030
Cytoband: 3q11.1
HGVS: NM_001174150.2(ARL13B):c.130+242T>C
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.