Variant (rsID / SNP)

rs3794109

rs3794109 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD44. Location: chromosome 11, position 35,192,279. Clinical significance in the table: association.

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Reference-table entries

CD44Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 11:35192279
Cytoband: 11p13
HGVS: NM_000610.4(CD44):c.68-5843A>G
Allele change: Silent

Associated conditions / phenotypes

Nephrolithiasis susceptibility caused by SLC26A1

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.