Variant (rsID / SNP)

rs2232613

rs2232613 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LBP. Location: chromosome 20, position 36,997,655. Clinical significance in the table: Uncertain significance.

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Reference-table entries

LBPUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 20:36997655
Cytoband: 20q11.23
HGVS: NM_004139.5(LBP):c.998C>T (p.Pro333Leu)
Allele change: Missense_P333L

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.