ClinVar Miner

Submissions for variant NC_000011.10:g.32438918G>A

gnomAD frequency: 0.16158  dbSNP: rs6508
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 RCV001514052 SCV001721798 benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718847 SCV005316019 benign not provided criteria provided, single submitter not provided

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