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Variant (rsID / SNP)

rs1801311

NDUFA6

rs1801311 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA6. Location: chromosome 22, position 42,486,723. The table records no clinical significance for this variant.

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Reference-table entries

NDUFA6Not classified
Variant type
missense_variant
Chromosome / position
22:42486723
HGVS
NM_002490.6,c.26C>T,p.Ala9Val
Allele change
Missense_A9V

Associated conditions / phenotypes

Schizophrenia

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.