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Variant (rsID / SNP)

rs7124513

NUDT8

rs7124513 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT8. Location: chromosome 11, position 67,395,714. The table records no clinical significance for this variant.

Reference-table entries

NUDT8Not classified
Variant type
synonymous_variant
Chromosome / position
11:67395714
HGVS
NM_001243750.2,c.414G>A,p.Glu138Glu
Allele change
Silent

Public references

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