ClinVar Miner

List of variants reported as likely benign for Danon disease by Illumina Laboratory Services, Illumina

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002294.3(LAMP2):c.*1701dup	rs373005118
NM_002294.3(LAMP2):c.*2148AT[9]	rs753399289
NM_002294.3(LAMP2):c.*3031dup	rs113549733
NM_002294.3(LAMP2):c.*3459GTT[3]	rs199705754

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