Variant (rsID / SNP)

rs121908177

rs121908177 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BBS2. Location: chromosome 16, position 56,536,702. Clinical significance in the table: Pathogenic.

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Reference-table entries

BBS2Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 16:56536702
Cytoband: 16q13
HGVS: NM_031885.5(BBS2):c.823C>T (p.Arg275Ter)
Allele change: Nonsense_R275X

Associated conditions / phenotypes

Bardet-Biedl syndrome 2|Bardet-Biedl syndrome|Retinitis pigmentosa 74|Bardet-Biedl syndrome 2|Retinal dystrophy

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.