List of variants in gene RYR1 reported as uncertain significance for long QT 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.9262G>A (p.Val3088Met)	rs145044872	0.00046
NM_000540.3(RYR1):c.5020G>A (p.Ala1674Thr)	rs1460141666	0.00001
NM_000540.3(RYR1):c.1354G>A (p.Glu452Lys)
NM_000540.3(RYR1):c.7880T>G (p.Val2627Gly)	rs747337318

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