Variant (rsID / SNP)

rs148146916

rs148146916 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSEN54, CASKIN2. Location: chromosome 17, position 73,513,281. Clinical significance in the table: Benign.

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Reference-table entries

TSEN54Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:73513281
Cytoband: 17q25.1
HGVS: NM_207346.3(TSEN54):c.325C>G (p.Arg109Gly)
Allele change: Missense_R109G

Associated conditions / phenotypes

Pontoneocerebellar hypoplasia

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.