RS397514919 TSC2

Health Risk Chr 16:2079326
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What This Variant Does
"CLNSIG=4
Associated Conditions
Tuberous sclerosis syndrome
Hereditary cancer-predisposing syndrome
Tuberous sclerosis syndrome
Hereditary cancer-predisposing syndrome
Other Variants in TSC2
rs137854083 rs45483392 rs45512692 rs137854337 rs45517179 rs28934872 rs45517214 rs121964862 rs45517148 rs45516293
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