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Variant (rsID / SNP)

rs2959656

MEN1

rs2959656 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MEN1. Location: chromosome 11, position 64,572,018. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

MEN1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
11:64572018
Cytoband
11q13.1
HGVS
NM_001370259.2(MEN1):c.1621= (p.Thr541=)
Allele change
Missense_T546A

Associated conditions / phenotypes

Primary hyperparathyroidism|Multiple endocrine neoplasia, type 1

Public references

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