Variant (rsID / SNP)

rs11922879

rs11922879 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAV3. Location: chromosome 3, position 8,775,702. Clinical significance in the table: Benign.

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Reference-table entries

CAV3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:8775702
Cytoband: 3p25.3
HGVS: NM_033337.3(CAV3):c.114+26G>A
Allele change: Silent

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.