ClinVar Miner

Submissions for variant NC_000011.10:g.2172610A>G

gnomAD frequency: 0.56453  dbSNP: rs10770141
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 RCV001509891 SCV001716797 benign Autosomal recessive DOPA responsive dystonia 2025-01-15 criteria provided, single submitter clinical testing
Center for Forensic Mental Health, Chiba University RCV003633586 SCV004543736 benign Schizophrenia criteria provided, single submitter case-control

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