Variant (rsID / SNP)

rs35789999

rs35789999 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ITPR1. Location: chromosome 3, position 4,714,920. Clinical significance in the table: Benign.

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Reference-table entries

ITPR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:4714920
Cytoband: 3p26.1
HGVS: NM_001378452.1(ITPR1):c.2305A>G (p.Met769Val)
Allele change: Missense_M754V

Associated conditions / phenotypes

Autosomal dominant cerebellar ataxia

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.