Variant (rsID / SNP)

rs199475901

rs199475901 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOD1. Location: chromosome 7, position 30,491,610. The table records no clinical significance for this variant.

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Reference-table entries

NOD1Not classified

Variant type: single nucleotide variant
Chromosome / position: 7:30491610
Cytoband: 7p14.3
HGVS: NM_006092.4(NOD1):c.1423C>T (p.Leu475Phe)
Allele change: Silent

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.