ClinVar Miner

Submissions for variant NC_000016.10:g.31096368=

gnomAD frequency: 0.68843  dbSNP: rs9923231
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
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000152659 SCV000202012 drug response Warfarin response 2006-12-16 no assertion criteria provided clinical testing

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