Variant (rsID / SNP)

rs4148946

rs4148946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHST3. Location: chromosome 10, position 73,770,073. Clinical significance in the table: Benign.

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Reference-table entries

CHST3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:73770073
Cytoband: 10q22.1
HGVS: NM_004273.5(CHST3):c.*1844C>T
Allele change: Silent

Associated conditions / phenotypes

Skeletal dysplasia|Larsen syndrome|Spondyloepiphyseal dysplasia with congenital joint dislocations|Spondyloepiphyseal dysplasia congenita

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.