Variant (rsID / SNP)

rs121908146

rs121908146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP3. Location: chromosome 1, position 247,588,067. Clinical significance in the table: Pathogenic.

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Reference-table entries

NLRP3Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:247588067
Cytoband: 1q44
HGVS: NM_001243133.2(NLRP3):c.1316C>T (p.Ala439Val)
Allele change: Missense_A441V

Associated conditions / phenotypes

Familial cold autoinflammatory syndrome 1|Cryopyrin associated periodic syndrome|Autoinflammatory syndrome

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.