Variant (rsID / SNP)

rs201499778

rs201499778 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNT12. Location: chromosome 9, position 101,599,425. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GALNT12Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 9:101599425
Cytoband: 9q22.33
HGVS: NM_024642.5(GALNT12):c.1207C>T (p.Arg403Cys)
Allele change: Missense_R403C

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

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.