Variant (rsID / SNP)

rs3204635

rs3204635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STAC3. Location: chromosome 12, position 57,637,593. Clinical significance in the table: Benign.

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Reference-table entries

STAC3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:57637593
Cytoband: 12q13.3
HGVS: NM_145064.3(STAC3):c.*2C>T
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.