Variant (rsID / SNP)

rs137853839

rs137853839 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OCRL. The table records no clinical significance for this variant.

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Reference-table entries

OCRLNot classified

Variant type: single nucleotide variant
Cytoband: Xq26.1
HGVS: NM_000276.4(OCRL):c.1369C>G (p.Arg457Gly)
Allele change: Missense_R458G

Associated conditions / phenotypes

Lowe syndrome

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.