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Variant (rsID / SNP)

rs76013375

UQCR10

rs76013375 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UQCR10. Location: chromosome 22, position 30,163,526. The table records no clinical significance for this variant.

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Reference-table entries

UQCR10Not classified
Variant type
missense_variant
Chromosome / position
22:30163526
HGVS
NM_013387.4,c.139A>G,p.Ile47Val
Allele change
Missense_I47V

Public references

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