Variant (rsID / SNP)

rs397977

rs397977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP5. Location: chromosome 19, position 56,539,240. The table records no clinical significance for this variant.

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Reference-table entries

NLRP5Not classified

Variant type: synonymous_variant
Chromosome / position: 19:56539240
HGVS: NM_153447.4,c.1641C>T,p.Asp547Asp
Allele change: Synonymous_D547D

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.