ClinVar Miner

List of variants reported as uncertain significance for inherited focal segmental glomerulosclerosis by Johns Hopkins Genomics, Johns Hopkins University

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_173689.7(CRB2):c.3754C>T (p.Arg1252Cys)	rs537738396	0.00006
NM_000278.5(PAX2):c.263C>T (p.Pro88Leu)	rs1845410479
NM_173689.7(CRB2):c.2803G>C (p.Gly935Arg)

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