List of variants in gene combination LOC126806068, RYR2 reported as uncertain significance for Arrhythmogenic right ventricular dysplasia 2

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.12919C>T (p.Arg4307Cys)	rs200092869	0.00038
NM_001035.3(RYR2):c.12492G>A (p.Gln4164=)	rs377293019	0.00024
NM_001035.3(RYR2):c.13137C>A (p.Ile4379=)	rs369917806	0.00021
NM_001035.3(RYR2):c.12858C>T (p.Ser4286=)	rs185482345	0.00004
NM_001035.3(RYR2):c.13175A>G (p.Lys4392Arg)	rs753733164	0.00003
NM_001035.3(RYR2):c.12404G>A (p.Arg4135His)	rs764202302	0.00001
NM_001035.3(RYR2):c.12627G>A (p.Ser4209=)	rs3753631	0.00001
NM_001035.3(RYR2):c.13220G>A (p.Ser4407Asn)	rs755585430	0.00001
NM_001035.3(RYR2):c.12712A>G (p.Ile4238Val)	rs1695382742

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