Variant (rsID / SNP)

rs10595

rs10595 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NDUFV3. Location: chromosome 21, position 44,324,365. The table records no clinical significance for this variant.

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Reference-table entries

NDUFV3Not classified

Variant type: missense_variant
Chromosome / position: 21:44324365
HGVS: NM_021075.4,c.1243G>A,p.Asp415Asn
Allele change: Missense_D415N

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.