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Variant (rsID / SNP)

rs12052989

SGO2

rs12052989 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SGO2. Location: chromosome 2, position 201,437,334. The table records no clinical significance for this variant.

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Reference-table entries

SGO2Not classified
Variant type
synonymous_variant
Chromosome / position
2:201437334
HGVS
NM_152524.6,c.2265T>C,p.Pro755Pro
Allele change
Synonymous_P755P

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.