ClinVar Miner

Submissions for variant NM_001371596.2(MFSD8):c.186A>G (p.Pro62=)

gnomAD frequency: 0.00002  dbSNP: rs750969105
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002153418 SCV002454612 likely benign Neuronal ceroid lipofuscinosis 7 2023-12-06 criteria provided, single submitter clinical testing

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