List of variants in gene EMP2 reported as uncertain significance for nephrotic syndrome, type 10

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001424.6(EMP2):c.497G>A (p.Arg166His)	rs138530114	0.00007
NM_001424.6(EMP2):c.188C>T (p.Ala63Val)
NM_001424.6(EMP2):c.427T>C (p.Tyr143His)

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