ClinVar Miner

Submissions for variant NC_000007.14:g.67771556T>C

gnomAD frequency: 0.61823  dbSNP: rs35629450
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Suna and Inan Kirac Foundation Neurodegeneration Research Laboratory, Koc University RCV001095454 SCV001251139 benign not specified 2020-04-02 no assertion criteria provided case-control

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