Variant (rsID / SNP)

rs140570189

rs140570189 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RLBP1. Location: chromosome 15, position 89,753,653. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RLBP1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:89753653
Cytoband: 15q26.1
HGVS: NM_000326.5(RLBP1):c.817C>T (p.Leu273Phe)
Allele change: Missense_L273F

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.