List of variants in gene RYR3 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001036.6(RYR3):c.9254C>G (p.Pro3085Arg)	rs61996335	0.00307
NM_001036.6(RYR3):c.7490A>G (p.Asn2497Ser)	rs61996331	0.00179
NM_001036.6(RYR3):c.10698G>A (p.Thr3566=)	rs200309704	0.00163
NM_001036.6(RYR3):c.6698G>A (p.Arg2233Gln)	rs199648816	0.00102
NM_001036.6(RYR3):c.6850G>A (p.Ala2284Thr)	rs201633381	0.00046
NM_001036.6(RYR3):c.30C>A (p.Asp10Glu)	rs761390620	0.00001

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