Variant (rsID / SNP)

rs2247341

rs2247341 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLBP. Location: chromosome 4, position 1,701,317. The table records no clinical significance for this variant.

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Reference-table entries

SLBPNot classified

Variant type: synonymous_variant
Chromosome / position: 4:1701317
HGVS: NM_006527.4,c.453C>T,p.Tyr151Tyr
Allele change: Synonymous_Y112Y

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.