Variant (rsID / SNP)

rs56379106

rs56379106 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAT1. Location: chromosome 8, position 18,079,746. Clinical significance in the table: Benign.

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Reference-table entries

NAT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:18079746
Cytoband: 8p22
HGVS: NM_000662.8(NAT1):c.190C>T (p.Arg64Trp)
Allele change: Missense_R64W

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.