Variant (rsID / SNP)

rs9542236

rs9542236 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B3GLCT. Location: chromosome 13, position 31,819,325. The table records no clinical significance for this variant.

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Reference-table entries

B3GLCTNot classified

Variant type: single nucleotide variant
Chromosome / position: 13:31819325
Cytoband: 13q12.3
HGVS: NM_194318.4(B3GLCT):c.271-1835T>C
Allele change: Silent

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.