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Variant (rsID / SNP)

rs4852974

NAT8B

rs4852974 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAT8B. Location: chromosome 2, position 73,927,931. The table records no clinical significance for this variant.

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Reference-table entries

NAT8BNot classified
Variant type
non_coding_transcript_exon_variant
Chromosome / position
2:73927931
HGVS
NR_132338.1,n.537T>C
Allele change
Silent

Public references

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