Variant (rsID / SNP)

rs251684

rs251684 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G4C. Location: chromosome 19, position 48,601,454. The table records no clinical significance for this variant.

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Reference-table entries

PLA2G4CNot classified

Variant type: synonymous_variant
Chromosome / position: 19:48601454
HGVS: NM_001159322.2,c.540A>G,p.Pro180Pro
Allele change: Synonymous_P170P

Associated conditions / phenotypes

Autism|Autism Spectrum Disorder

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.