ClinVar Miner

List of variants in gene combination FN1, LOC126806496 reported as pathogenic for fibronectin glomerulopathy

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_212482.4(FN1):c.5921T>C (p.Leu1974Pro)	rs137854487
NM_212482.4(FN1):c.5921T>G (p.Leu1974Arg)	rs137854487

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