RS28931612 MEN1

Health Risk Chr 11:64810034
Upload your DNA to see your genotype for this variant.
What This Variant Does
"NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP [OMIM:PARATHYROID...
Associated Conditions
Parathyroid adenoma
somatic
Multiple endocrine neoplasia
type 1
Parathyroid adenoma
somatic
Multiple endocrine neoplasia
type 1
Other Variants in MEN1
rs104894256 rs397515385 rs104894258 rs1555164986 rs869025185 rs104894259 rs104894260 rs104894261 rs104894266 rs104894267
Ask Dr. Hemsworth about this variant