ClinVar Miner

List of variants reported as not provided for inherited focal segmental glomerulosclerosis by GenomeConnect, ClinGen

Included ClinVar conditions (11):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_018685.5(ANLN):c.31C>T (p.Arg11Ter)	rs200989750	0.00023
NM_004998.4(MYO1E):c.1415C>T (p.Ala472Val)	rs371914169	0.00001

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