Variant (rsID / SNP)

rs41306504

rs41306504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GALNT12. Location: chromosome 9, position 101,594,103. 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: 9:101594103
Cytoband: 9q22.33
HGVS: NM_024642.5(GALNT12):c.781G>A (p.Asp261Asn)
Allele change: Missense_D261N

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome|Colorectal cancer, susceptibility to, 1

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.