Variant (rsID / SNP)

rs150884181

rs150884181 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBLIF. Location: chromosome 11, position 59,610,581. Clinical significance in the table: Benign.

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Reference-table entries

CBLIFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:59610581
Cytoband: 11q12.1
HGVS: NM_005142.3(CBLIF):c.290T>C (p.Met97Thr)
Allele change: Missense_M97T

Associated conditions / phenotypes

Hereditary intrinsic factor deficiency

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.