ClinVar Miner

List of variants reported as pathogenic for inherited focal segmental glomerulosclerosis by 3billion

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_000278.5(PAX2):c.76dup (p.Val26fs)	rs75462234
NM_022489.4(INF2):c.640C>T (p.Arg214Cys)	rs912928648
NM_022489.4(INF2):c.653G>A (p.Arg218Gln)	rs267607183

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