Variant (rsID / SNP)

rs200387097

rs200387097 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA10. Location: chromosome 2, position 240,954,203. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NDUFA10Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:240954203
Cytoband: 2q37.3
HGVS: NM_004544.4(NDUFA10):c.622G>C (p.Asp208His)
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.