Variant (rsID / SNP)

rs145241128

rs145241128 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B4GALT1. Location: chromosome 9, position 33,135,214. Clinical significance in the table: Likely benign.

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Reference-table entries

B4GALT1Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:33135214
Cytoband: 9p21.1
HGVS: NM_001497.4(B4GALT1):c.621G>A (p.Leu207=)
Allele change: Synonymous_L207L

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.