Variant (rsID / SNP)

rs12461110

rs12461110 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP11. Location: chromosome 19, position 56,320,663. The table records no clinical significance for this variant.

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Reference-table entries

NLRP11Not classified

Variant type: missense_variant
Chromosome / position: 19:56320663
HGVS: NM_001394894.2,c.1313C>T,p.Pro438Leu
Allele change: Missense_P339L

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.