ClinVar Miner

Submissions for variant NM_001036.6(RYR3):c.4529T>C (p.Val1510Ala)

gnomAD frequency: 0.00001  dbSNP: rs431825175
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
Johns Hopkins Genetic Resources Core Facility; Johns Hopkins University RCV000083247 SCV000115321 not provided not provided no assertion provided not provided

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