Variant (rsID / SNP)

rs147070468

rs147070468 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B4GALT1. Location: chromosome 9, position 33,113,786. Clinical significance in the table: Benign.

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Reference-table entries

B4GALT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:33113786
Cytoband: 9p21.1
HGVS: NM_001497.4(B4GALT1):c.1050A>G (p.Glu350=)
Allele change: Synonymous_E350E

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.