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Variant (rsID / SNP)

rs116157972

MRPS16

rs116157972 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPS16. Location: chromosome 10, position 75,011,683. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MRPS16Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
10:75011683
Cytoband
10q22.2
HGVS
NM_016065.4(MRPS16):c.112C>A (p.His38Asn)
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.