Variant (rsID / SNP)

rs3135499

rs3135499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOD2. Location: chromosome 16, position 50,766,127. Clinical significance in the table: Benign.

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Reference-table entries

NOD2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:50766127
Cytoband: 16q12.1
HGVS: NM_001370466.1(NOD2):c.*397A>C
Allele change: Silent

Associated conditions / phenotypes

Blau syndrome|Inflammatory bowel disease 1|Leprosy, susceptibility to, 1

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.