Variant (rsID / SNP)

rs9823911

rs9823911 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAALADL2. Location: chromosome 3, position 174,814,738. The table records no clinical significance for this variant.

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Reference-table entries

NAALADL2Not classified

Variant type: missense_variant
Chromosome / position: 3:174814738
HGVS: NM_207015.3,c.202G>A,p.Gly68Ser
Allele change: Missense_G68S

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.