List of variants in gene RBM20 reported as benign by Eurofins NTD LLC (GA)

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001134363.3(RBM20):c.90G>A (p.Arg30=)	rs35141404	0.20903
NM_001134363.3(RBM20):c.1881-3C>T	rs138436392	0.00575
NM_001134363.3(RBM20):c.2318A>G (p.Lys773Arg)	rs181769913	0.00324
NM_001134363.3(RBM20):c.3265C>G (p.Pro1089Ala)	rs147356378	0.00252
NM_001134363.3(RBM20):c.3170G>A (p.Arg1057Gln)	rs188054898	0.00107
NM_001134363.3(RBM20):c.2303= (p.Ser768=)	rs1417635

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