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Variant (rsID / SNP)

rs35181012

NUDT8

rs35181012 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT8. Location: chromosome 11, position 67,395,634. The table records no clinical significance for this variant.

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Reference-table entries

NUDT8Not classified
Variant type
missense_variant
Chromosome / position
11:67395634
HGVS
NM_001243750.2,c.494G>A,p.Arg165His
Allele change
Silent

Public references

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