Variant (rsID / SNP)

rs148679749

rs148679749 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPL3. Location: chromosome 3, position 131,181,683. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MRPL3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:131181683
Cytoband: 3q22.1
HGVS: NM_007208.4(MRPL3):c.931G>A (p.Gly311Ser)
Allele change: Missense_G311S

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.