Variant (rsID / SNP)

rs12660274

rs12660274 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCNT2. Location: chromosome 6, position 10,555,982. Clinical significance in the table: Benign.

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Reference-table entries

GCNT2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:10555982
Cytoband: 6p24.3
HGVS: NM_145649.5(GCNT2):c.925+25913G>T
Allele change: Silent

Associated conditions / phenotypes

I blood group system

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.