Variant (rsID / SNP)

rs3813535

rs3813535 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STON2. Location: chromosome 14, position 81,744,736. The table records no clinical significance for this variant.

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Reference-table entries

STON2Not classified

Variant type: missense_variant
Chromosome / position: 14:81744736
HGVS: NM_001366849.2,c.1090T>C,p.Ser364Pro
Allele change: Missense_S307P

Associated conditions / phenotypes

Schizophrenia 11

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.