Variant (rsID / SNP)

rs116677006

rs116677006 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RLBP1. Location: chromosome 15, position 89,758,328. Clinical significance in the table: Uncertain significance.

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Reference-table entries

RLBP1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:89758328
Cytoband: 15q26.1
HGVS: NM_000326.5(RLBP1):c.488T>C (p.Ile163Thr)
Allele change: Missense_I163T

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.