ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.999+44T>C

gnomAD frequency: 0.18118  dbSNP: rs3729810
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
PreventionGenetics, part of Exact Sciences RCV000246179 SCV000303261 benign not specified criteria provided, single submitter clinical testing

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