ClinVar Miner

Submissions for variant NC_000007.14:g.67770277A>G

gnomAD frequency: 0.31723  dbSNP: rs6942794
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001095451 SCV001251136 benign not specified 2020-04-02 criteria provided, single submitter case-control

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