Variant (rsID / SNP)
rs3812694
rs3812694 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NPFFR1. Location: chromosome 10, position 72,015,573. The table records no clinical significance for this variant.
Reference-table entries
NPFFR1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:72015573
- HGVS
- NM_022146.5,c.433A>C,p.Ile145Leu
- Allele change
- Missense_I145L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.