RS267606569 AIP

Health Risk Chr 11:67490383
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What This Variant Does
"CLNSIG=4
Associated Conditions
Somatotroph adenoma
Hereditary cancer-predisposing syndrome
Somatotroph adenoma
Hereditary cancer-predisposing syndrome
Other Variants in AIP
rs104894194 rs104894195 rs267606567 rs267606580 rs267606559 rs121908356 rs104894190 rs121908357 rs1063385 rs267606541
Ask Dr. Hemsworth about this variant