Variant (rsID / SNP)

rs237867

rs237867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CAV3. Location: chromosome 3, position 8,775,295. Clinical significance in the table: Likely benign.

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Reference-table entries

CAV3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:8775295
Cytoband: 3p25.3
HGVS: NM_033337.2(CAV3):c.-268C>T

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.