Variant (rsID / SNP)

rs35107257

rs35107257 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OCLN. Location: chromosome 5, position 68,805,616. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

OCLNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:68805616
Cytoband: 5q13.2
HGVS: NM_001205254.2(OCLN):c.699G>A (p.Leu233=)
Allele change: Synonymous_L233L

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.