List of variants in gene RYR1 reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.2871-5C>T	rs45585535	0.03110
NM_000540.3(RYR1):c.5360C>T (p.Pro1787Leu)	rs34934920	0.01583
NM_000540.3(RYR1):c.10747G>C (p.Glu3583Gln)	rs55876273	0.01228
NM_000540.3(RYR1):c.1923C>G (p.Thr641=)	rs116591968	0.00404
NM_000540.3(RYR1):c.6732G>A (p.Arg2244=)	rs78915828	0.00390
NM_000540.3(RYR1):c.14505G>A (p.Gly4835=)	rs118126378	0.00334
NM_000540.3(RYR1):c.4178A>G (p.Lys1393Arg)	rs137933390	0.00282
NM_000540.3(RYR1):c.9555-9G>A	rs149569999	0.00180
NM_000540.3(RYR1):c.725+6G>A	rs201679831	0.00111

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