Variant (rsID / SNP)

rs376338190

rs376338190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPS16. Location: chromosome 10, position 75,011,732. Clinical significance in the table: Likely benign.

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Reference-table entries

MRPS16Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:75011732
Cytoband: 10q22.2
HGVS: NM_016065.4(MRPS16):c.63T>C (p.Leu21=)
Allele change: Silent

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.