Variant (rsID / SNP)

rs34218557

rs34218557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BBS9. Location: chromosome 7, position 33,397,476. Clinical significance in the table: Benign.

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Reference-table entries

BBS9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:33397476
Cytoband: 7p14.3
HGVS: NM_198428.3(BBS9):c.1562G>A (p.Arg521Gln)
Allele change: Silent

Associated conditions / phenotypes

Bardet-Biedl syndrome|Bardet-Biedl syndrome 1|Bardet-Biedl syndrome 9

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.