Variant (rsID / SNP)

rs2271909

rs2271909 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPS16. Location: chromosome 10, position 75,012,248. Clinical significance in the table: Benign.

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Reference-table entries

MRPS16Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:75012248
Cytoband: 10q22.2
HGVS: NM_016065.4(MRPS16):c.-8G>C
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.