Variant (rsID / SNP)

rs11564538

rs11564538 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G4C. Location: chromosome 19, position 48,601,512. The table records no clinical significance for this variant.

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Reference-table entries

PLA2G4CNot classified

Variant type: missense_variant
Chromosome / position: 19:48601512
HGVS: NM_001159322.2,c.482C>T,p.Pro161Leu
Allele change: Missense_P151L

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.