Variant (rsID / SNP)

rs4861597

rs4861597 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to STOX2. Location: chromosome 4, position 184,931,818. The table records no clinical significance for this variant.

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Reference-table entries

STOX2Not classified

Variant type: synonymous_variant
Chromosome / position: 4:184931818
HGVS: NM_020225.3,c.1827G>A,p.Thr609Thr
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.