Variant (rsID / SNP)

rs138593604

rs138593604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCNT2. Location: chromosome 6, position 10,557,417. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GCNT2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:10557417
Cytoband: 6p24.3
HGVS: NM_001491.3(GCNT2):c.761A>G (p.His254Arg)
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.