List of variants in gene RYR2 reported by CSER _CC_NCGL, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.8162T>C (p.Ile2721Thr)	rs201500134	0.00069
NM_001035.3(RYR2):c.3038G>A (p.Arg1013Gln)	rs149514924	0.00063
NM_001035.3(RYR2):c.1396C>G (p.Pro466Ala)	rs376612295	0.00007
NM_001035.3(RYR2):c.5822G>A (p.Arg1941His)	rs373600053	0.00007
NM_001035.3(RYR2):c.13666G>A (p.Ala4556Thr)	rs189345192	0.00003
NM_001035.3(RYR2):c.7493C>T (p.Ala2498Val)	rs374191985	0.00003
NM_001035.3(RYR2):c.3484G>A (p.Val1162Met)	rs377030538	0.00002
NM_001035.3(RYR2):c.556G>A (p.Val186Met)	rs201211033	0.00002
NM_001035.3(RYR2):c.11968G>A (p.Val3990Ile)	rs1210103464	0.00001
NM_001035.3(RYR2):c.12023A>G (p.Asn4008Ser)	rs1330847491	0.00001
NM_001035.3(RYR2):c.2402G>T (p.Arg801Leu)	rs371157868	0.00001
NM_001035.3(RYR2):c.4196C>A (p.Thr1399Lys)	rs75901196

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