ClinVar Miner

Submissions for variant NM_001124758.3(SPNS2):c.935+26T>C

gnomAD frequency: 0.99161  dbSNP: rs9892232
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001612262 SCV001839462 benign not provided 2021-05-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810133 SCV002057644 benign Hearing loss, autosomal recessive 115 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001612262 SCV005252731 benign not provided criteria provided, single submitter not provided

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