Variant (rsID / SNP)

rs61733987

rs61733987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA1A. Location: chromosome 3, position 119,327,670. The table records no clinical significance for this variant.

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Reference-table entries

PLA1ANot classified

Variant type: missense_variant
Chromosome / position: 3:119327670
HGVS: NM_015900.4,c.329G>A,p.Arg110His
Allele change: Silent

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.