RS104894261 MEN1

Health Risk Chr 11:64804588
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What This Variant Does
"[OMIM:?]
Associated Conditions
Multiple endocrine neoplasia
type 1
Hereditary cancer-predisposing syndrome
Neuroendocrine tumor of pancreas
Familial hyperparathyroidism or Hypocalciuric hypercalcaemia
Multiple endocrine neoplasia
type 1
Hereditary cancer-predisposing syndrome
Neuroendocrine tumor of pancreas
Familial hyperparathyroidism or Hypocalciuric hypercalcaemia
Other Variants in MEN1
rs104894256 rs397515385 rs104894258 rs1555164986 rs869025185 rs104894259 rs104894260 rs28931612 rs104894266 rs104894267
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