Variant (rsID / SNP)

rs35502837

rs35502837 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMARCB1. Location: chromosome 22, position 24,143,573. Clinical significance in the table: Likely benign.

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Reference-table entries

SMARCB1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 22:24143573
Cytoband: 22q11.23
HGVS: NM_003073.5(SMARCB1):c.500+305C>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.