ClinVar Miner

Submissions for variant NM_002361.4(MAG):c.1716+18G>C

gnomAD frequency: 0.00401  dbSNP: rs10419210
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002218740 SCV002362667 benign Hereditary spastic paraplegia 75 2023-12-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002218740 SCV002797979 likely benign Hereditary spastic paraplegia 75 2021-09-27 criteria provided, single submitter clinical testing

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