ClinVar Miner

List of variants in gene RYR3 reported as likely pathogenic

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001036.6(RYR3):c.3092A>T (p.Lys1031Met)	rs753104655	0.00006
NM_001036.6(RYR3):c.4505G>T (p.Arg1502Leu)	rs545597409

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