Variant (rsID / SNP)

rs324419

rs324419 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAAH. Location: chromosome 1, position 46,871,986. The table records no clinical significance for this variant.

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Reference-table entries

FAAHNot classified

Variant type: synonymous_variant
Chromosome / position: 1:46871986
HGVS: NM_001441.3,c.897T>C,p.Cys299Cys
Allele change: Synonymous_C299C

Associated conditions / phenotypes

Body Mass Index Quantitative Trait Locus 11|Parkinson Disease, Late-Onset

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.