ClinVar Miner

Submissions for variant NM_001126131.1(POLG):c.[1491G>C(;)2243G>C]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dept. of Medical Genetics, Telemark Hospital Trust, Telemark Hospital Trust RCV000144870 SCV000172142 uncertain significance Charcot-Marie-Tooth disease 2013-11-01 no assertion criteria provided research

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