Variant (rsID / SNP)

rs78496674

rs78496674 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NUDT18. Location: chromosome 8, position 21,967,407. The table records no clinical significance for this variant.

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Reference-table entries

NUDT18Not classified

Variant type: upstream_gene_variant
Chromosome / position: 8:21967407
HGVS: NM_024815.4,c.-594A>G

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.