Variant (rsID / SNP)

rs59362219

rs59362219 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNT12. Location: chromosome 9, position 101,589,211. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GALNT12Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:101589211
Cytoband: 9q22.33
HGVS: NM_024642.5(GALNT12):c.719C>T (p.Pro240Leu)
Allele change: Missense_P240L

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Breast neoplasm

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.