Variant (rsID / SNP)

rs104894263

rs104894263 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEN1. Location: chromosome 11, position 64,577,167. Clinical significance in the table: Pathogenic.

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Reference-table entries

MEN1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 11:64577167
Cytoband: 11q13.1
HGVS: NM_001370259.2(MEN1):c.415C>G (p.His139Asp)
Allele change: Missense_H139D

Associated conditions / phenotypes

Multiple endocrine neoplasia, type 1|Hereditary cancer-predisposing 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.