Variant (rsID / SNP)

rs9289390

rs9289390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPL3. Location: chromosome 3, position 131,219,070. Clinical significance in the table: Benign.

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Reference-table entries

MRPL3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:131219070
Cytoband: 3q22.1
HGVS: NM_007208.4(MRPL3):c.369+204G>A
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.