Variant (rsID / SNP)

rs34076756

rs34076756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA9. Location: chromosome 12, position 4,791,451. Clinical significance in the table: Benign.

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Reference-table entries

NDUFA9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 12:4791451
Cytoband: 12p13.32
HGVS: NM_005002.5(NDUFA9):c.881C>T (p.Pro294Leu)
Allele change: Missense_P294L

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.