Variant (rsID / SNP)

rs115856545

rs115856545 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CANT1. Location: chromosome 17, position 76,988,803. Clinical significance in the table: Benign.

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Reference-table entries

CANT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:76988803
Cytoband: 17q25.3
HGVS: NM_001159773.2(CANT1):c.*829G>A
Allele change: Silent

Associated conditions / phenotypes

Desbuquois dysplasia 1

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.