ClinVar Miner

Submissions for variant NM_003901.4(SGPL1):c.1566+32T>G

gnomAD frequency: 0.74750  dbSNP: rs923177
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001721588 SCV001948350 benign not provided 2021-05-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001807527 SCV002055183 benign Nephrotic syndrome 14 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001721588 SCV005321221 benign not provided criteria provided, single submitter not provided

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