List of variants in gene RYR1 reported as uncertain significance by Institute of Human Genetics, University of Wuerzburg

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000540.3(RYR1):c.396C>T (p.Phe132=)	rs376494617	0.00005
NM_000540.3(RYR1):c.10520C>T (p.Thr3507Met)	rs371839408	0.00004
NM_000540.3(RYR1):c.15088C>T (p.Arg5030Cys)	rs374070555	0.00001
NC_000019.10:g.38455669G>A
NM_000540.3(RYR1):c.11531A>T (p.Asn3844Ile)

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