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Variant (rsID / SNP)

rs35211634

CBLIF

rs35211634 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBLIF. Location: chromosome 11, position 59,612,859. 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
11:59612859
Cytoband
11q12.1
HGVS
NM_005142.3(CBLIF):c.68A>G (p.Gln23Arg)
Allele change
Missense_Q23R

Associated conditions / phenotypes

Intrinsic factor deficiency, congenital, susceptibility to|Hereditary intrinsic factor deficiency

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.