Variant (rsID / SNP)

rs324420

rs324420 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAAH. Location: chromosome 1, position 46,870,761. Clinical significance in the table: Benign.

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Reference-table entries

FAAHBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:46870761
Cytoband: 1p33
HGVS: NM_001441.3(FAAH):c.385C>A (p.Pro129Thr)
Allele change: Missense_P129T

Associated conditions / phenotypes

FAAH POLYMORPHISM

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.