Variant (rsID / SNP)

rs151340626

rs151340626 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCN5. Clinical significance in the table: Pathogenic.

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Reference-table entries

CLCN5Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xp11.23
HGVS: NM_001127898.4(CLCN5):c.941C>T (p.Ser314Leu)
Allele change: Missense_S314L

Associated conditions / phenotypes

Hypophosphatemic rickets, X-linked recessive|Dent disease type 1

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.