Variant (rsID / SNP)

rs2229948

rs2229948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CACNA1B. Location: chromosome 9, position 141,008,876. The table records no clinical significance for this variant.

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Reference-table entries

CACNA1BNot classified

Variant type: synonymous_variant
Chromosome / position: 9:141008876
HGVS: NM_000718.4,c.5583C>T,p.Phe1861Phe
Allele change: Synonymous_F1861F

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.