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Variant (rsID / SNP)

rs199968321

SPTBN2

rs199968321 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN2. Location: chromosome 11, position 66,472,775. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SPTBN2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
11:66472775
Cytoband
11q13.2
HGVS
NM_006946.4(SPTBN2):c.1972C>T (p.Arg658Trp)
Allele change
Missense_R658W

Associated conditions / phenotypes

Autosomal dominant cerebellar ataxia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.