Variant (rsID / SNP)

rs1678868

rs1678868 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFA11. Location: chromosome 19, position 5,892,954. The table records no clinical significance for this variant.

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Reference-table entries

NDUFA11Not classified

Variant type: missense_variant
Chromosome / position: 19:5892954
HGVS: NM_001193375.3,c.661A>G,p.Thr221Ala
Allele change: Missense_T221A

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.