Variant (rsID / SNP)

rs148402231

rs148402231 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFB9. Location: chromosome 8, position 125,562,065. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NDUFB9Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 8:125562065
Cytoband: 8q24.13
HGVS: NM_005005.3(NDUFB9):c.472C>G (p.Arg158Gly)
Allele change: Missense_R147G

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.