List of variants in gene RBM20 reported as uncertain significance by Genetics and Genomics Program, Sidra Medicine

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001134363.3(RBM20):c.150_153del (p.Pro52fs)	rs1861841498
NM_001134363.3(RBM20):c.2004C>A (p.Asp668Glu)	rs749563704
NM_001134363.3(RBM20):c.3047G>C (p.Gly1016Ala)	rs540014314
NM_001134363.3(RBM20):c.3517G>A (p.Glu1173Lys)	rs542297252

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