List of variants in gene RYR2 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_001035.3(RYR2):c.3380A>G (p.Glu1127Gly)	rs200525962	0.00048
NM_001035.3(RYR2):c.5774T>C (p.Ile1925Thr)	rs761505396	0.00003
NM_001035.3(RYR2):c.4850G>C (p.Trp1617Ser)	rs1677785308	0.00001
NM_001035.3(RYR2):c.5680C>A (p.Leu1894Ile)	rs555692728	0.00001

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