Variant (rsID / SNP)

rs3097644

rs3097644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BRD2. Location: chromosome 6, position 32,945,530. Clinical significance in the table: Benign.

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Reference-table entries

BRD2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:32945530
Cytoband: 6p21.32
HGVS: NM_005104.4(BRD2):c.1330-4G>C
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.