Variant (rsID / SNP)

rs2296568

rs2296568 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNNM2. Location: chromosome 10, position 104,836,940. Clinical significance in the table: Benign.

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Reference-table entries

CNNM2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:104836940
Cytoband: 10q24.32
HGVS: NM_017649.5(CNNM2):c.*3C>T
Allele change: Silent

Associated conditions / phenotypes

Renal hypomagnesemia 6

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.