Variant (rsID / SNP)

rs45551835

rs45551835 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CUBN. Location: chromosome 10, position 16,932,384. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CUBNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:16932384
Cytoband: 10p13
HGVS: NM_001081.4(CUBN):c.8741C>T (p.Ala2914Val)
Allele change: Missense_A2914V

Associated conditions / phenotypes

Imerslund-Grasbeck syndrome type 1|Imerslund-Grasbeck syndrome

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.