List of variants in gene LAMB2 reported as uncertain significance for Nephrotic syndrome

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_002292.4(LAMB2):c.3355G>A (p.Gly1119Ser)	rs199570781	0.00011
NM_002292.4(LAMB2):c.3232C>T (p.Arg1078Cys)	rs143284092	0.00006
NM_002292.4(LAMB2):c.4573+5G>A	rs372438959	0.00006
NM_002292.3(LAMB2):c.-241T>C	rs886058680	0.00004
NM_002292.4(LAMB2):c.4489A>G (p.Lys1497Glu)	rs771769006	0.00001
NM_002292.3(LAMB2):c.-200C>T	rs886058679
NM_002292.3(LAMB2):c.-252T>C	rs886058681
NM_002292.3(LAMB2):c.-279A>T	rs886058682
NM_002292.4(LAMB2):c.1104T>G (p.Asn368Lys)	rs2045467851
NM_002292.4(LAMB2):c.2224G>A (p.Ala742Thr)	rs959473971
NM_002292.4(LAMB2):c.2344C>T (p.Pro782Ser)	rs199837675
NM_002292.4(LAMB2):c.2884+15del	rs769133638

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