List of variants in gene RYR3 reported as benign for not provided

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001036.6(RYR3):c.4921C>T (p.Arg1641Cys)	rs4780144	0.86593
NM_001036.6(RYR3):c.10881A>G (p.Ala3627=)	rs2288614	0.68953
NM_001036.6(RYR3):c.6620-3C>T	rs2293028	0.29882
NM_001036.6(RYR3):c.6717G>A (p.Gly2239=)	rs2293027	0.15591
NM_001036.6(RYR3):c.12516G>C (p.Val4172=)	rs75286462	0.03322
NM_001036.6(RYR3):c.8997C>T (p.Pro2999=)	rs8041960	0.02841
NM_001036.6(RYR3):c.8998A>G (p.Ile3000Val)	rs10851894	0.02469
NM_001036.6(RYR3):c.4622+14C>T	rs182323574	0.00094
GRCh37/hg19 15q13.3-14(chr15:33481944-33687915)x3
GRCh37/hg19 15q14(chr15:34030192-34071305)x1
NM_001036.6(RYR3):c.10816-9del	rs35254800
NM_001036.6(RYR3):c.13314AGA[2] (p.Glu4441del)	rs3217346
NM_001036.6(RYR3):c.8136+9C>G	rs41279216

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