Variant (rsID / SNP)

rs117452684

rs117452684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BNC2. Location: chromosome 9, position 16,419,519. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

BNC2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:16419519
Cytoband: 9p22.3
HGVS: NM_017637.6(BNC2):c.2768C>T (p.Ala923Val)
Allele change: Missense_A923V

Associated conditions / phenotypes

Hypotension

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.