Variant (rsID / SNP)

rs79527490

rs79527490 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BIN1. Location: chromosome 2, position 127,811,774. Clinical significance in the table: Benign.

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Reference-table entries

BIN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:127811774
Cytoband: 2q14.3
HGVS: NM_139343.3(BIN1):c.1132-186G>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.