Variant (rsID / SNP)

rs910857

rs910857 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC52A3. Location: chromosome 20, position 741,847. Clinical significance in the table: Benign.

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Reference-table entries

SLC52A3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:741847
Cytoband: 20p13
HGVS: NM_033409.4(SLC52A3):c.1233T>C (p.Ser411=)
Allele change: Synonymous_S411S

Associated conditions / phenotypes

Brown-Vialetto-van Laere syndrome 1|Progressive bulbar palsy of childhood

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.