List of variants in gene RYR2 reported by Institute of Human Genetics, University of Leipzig Medical Center

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.12159G>A (p.Glu4053=)	rs41267517	0.00116
NM_001035.3(RYR2):c.4273A>G (p.Thr1425Ala)	rs776046135	0.00009
NM_001035.3(RYR2):c.1396C>G (p.Pro466Ala)	rs376612295	0.00007
NM_001035.3(RYR2):c.1249C>G (p.Arg417Gly)	rs564822776	0.00004
NM_001035.3(RYR2):c.1031_1035del (p.Lys344fs)	rs2150146622
NM_001035.3(RYR2):c.14801C>A (p.Thr4934Lys)
NM_001035.3(RYR2):c.6202C>T (p.Arg2068Ter)	rs1679845277
NM_001035.3(RYR2):c.6532G>A (p.Val2178Ile)	rs794728821
NM_001035.3(RYR2):c.8659dup (p.Glu2887fs)	rs1685193967

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