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Variant (rsID / SNP)

rs104895452

NOD2

rs104895452 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOD2. Location: chromosome 16, position 50,756,571. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

NOD2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:50756571
Cytoband
16q12.1
HGVS
NM_001370466.1(NOD2):c.2672C>A (p.Ala891Asp)
Allele change
Missense_A918D

Associated conditions / phenotypes

Blau syndrome|Inflammatory bowel disease 1|Blau syndrome|Inflammatory bowel disease 1|Autoinflammatory syndrome

Public references

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