Variant (rsID / SNP)

rs12408380

rs12408380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ST6GALNAC3. Location: chromosome 1, position 76,775,246. The table records no clinical significance for this variant.

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Reference-table entries

ST6GALNAC3Not classified

Variant type: start_lost
Chromosome / position: 1:76775246
HGVS: NM_001349111.2,c.3G>A,p.Met1?
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.