List of variants in gene combination LOC126806067, RYR2 reported as benign for heart conduction disease

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.3849A>G (p.Leu1283=)	rs143603583	0.00282
NM_001035.3(RYR2):c.4068C>T (p.Pro1356=)	rs199821105	0.00240
NM_001035.3(RYR2):c.3888C>T (p.Asn1296=)	rs373721253	0.00046
NM_001035.3(RYR2):c.4094C>T (p.Ala1365Val)	rs373261115	0.00010
NM_001035.3(RYR2):c.4044G>A (p.Lys1348=)	rs755391572	0.00009
NM_001035.3(RYR2):c.3933G>A (p.Ala1311=)	rs573948177	0.00002

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