Variant (rsID / SNP)

rs11548454

rs11548454 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LGALS3BP. Location: chromosome 17, position 76,972,231. The table records no clinical significance for this variant.

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Reference-table entries

LGALS3BPNot classified

Variant type: synonymous_variant
Chromosome / position: 17:76972231
HGVS: NM_005567.4,c.60C>T,p.Asn20Asn
Allele change: Synonymous_N20N

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.