List of variants in gene RYR2 reported as uncertain significance by Medical Research Institute, Tokyo Medical and Dental University

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.5278C>T (p.Arg1760Trp)	rs776550479	0.00003
NM_001035.3(RYR2):c.8470C>T (p.Arg2824Trp)	rs796052204	0.00002
NM_001035.3(RYR2):c.11017C>T (p.Arg3673Trp)	rs796052205
NM_001035.3(RYR2):c.12272C>T (p.Ala4091Val)	rs794728783
NM_001035.3(RYR2):c.1259G>A (p.Arg420Gln)	rs794728721
NM_001035.3(RYR2):c.1298T>C (p.Leu433Pro)	rs121918602
NM_001035.3(RYR2):c.13780A>C (p.Lys4594Gln)	rs796052207
NM_001035.3(RYR2):c.497C>G (p.Ser166Cys)	rs796052203

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