Variant (rsID / SNP)

rs269912

rs269912 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP2. Location: chromosome 19, position 55,481,398. The table records no clinical significance for this variant.

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Reference-table entries

NLRP2Not classified

Variant type: synonymous_variant
Chromosome / position: 19:55481398
HGVS: NM_001174081.3,c.15G>A,p.Ala5Ala
Allele change: Synonymous_A5A

Associated conditions / phenotypes

Synonymous_A5A

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.