ClinVar Miner

Submissions for variant NM_000405.5(GM2A):c.427-22C>T

gnomAD frequency: 0.00131  dbSNP: rs183697013
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
Mayo Clinic Laboratories, Mayo Clinic RCV000675623 SCV000801323 likely benign not provided 2017-11-17 no assertion criteria provided clinical testing

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