Variant (rsID / SNP)

rs3738298

rs3738298 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCND3. Location: chromosome 1, position 112,329,551. Clinical significance in the table: Benign.

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Reference-table entries

KCND3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:112329551
Cytoband: 1p13.2
HGVS: NM_001378969.1(KCND3):c.1269+15C>A
Allele change: Silent

Associated conditions / phenotypes

Spinocerebellar ataxia type 19/22

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.