Variant (rsID / SNP)

rs9866564

rs9866564 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAALADL2. Location: chromosome 3, position 175,345,143. The table records no clinical significance for this variant.

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Reference-table entries

NAALADL2Not classified

Variant type: missense_variant
Chromosome / position: 3:175345143
HGVS: NM_207015.3,c.1865C>G,p.Pro622Arg
Allele change: Missense_P622R

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.