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Variant (rsID / SNP)

rs78620448

GAL3ST2

rs78620448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GAL3ST2. Location: chromosome 2, position 242,716,400. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

GAL3ST2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:242716400
Cytoband
2q37.3
HGVS
NM_022134.3(GAL3ST2):c.29+1G>A
Allele change
Silent

Public references

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