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Variant (rsID / SNP)

rs1470590

ST6GAL2

rs1470590 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ST6GAL2. Location: chromosome 2, position 107,423,395. The table records no clinical significance for this variant.

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Reference-table entries

ST6GAL2Not classified
Variant type
synonymous_variant
Chromosome / position
2:107423395
HGVS
NM_001142351.2,c.1329A>C,p.Ile443Ile
Allele change
Synonymous_I443I

Public references

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