Variant (rsID / SNP)

rs2060113

rs2060113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FAAH2. The table records no clinical significance for this variant.

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Reference-table entries

FAAH2Not classified

Variant type: intron_variant
HGVS: NM_174912.4,c.1423+3431C>T
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.