List of variants in gene combination LOC126806433, TTN reported by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.7061G>A (p.Arg2354His)	rs75031300	0.00287
NM_001267550.2(TTN):c.7060C>T (p.Arg2354Cys)	rs145039979	0.00021
NM_001267550.2(TTN):c.7469G>A (p.Arg2490His)	rs148920986	0.00010
NM_001267550.2(TTN):c.6950G>A (p.Arg2317His)	rs764882950	0.00006
NM_001267550.2(TTN):c.7023C>T (p.Asp2341=)	rs761409144	0.00006
NM_001267550.2(TTN):c.6820C>G (p.Gln2274Glu)	rs145649088	0.00003
NM_001267550.2(TTN):c.6942T>C (p.Ile2314=)	rs762511156	0.00002
NM_001267550.2(TTN):c.7392T>C (p.Leu2464=)	rs565784637	0.00002
NM_001267550.2(TTN):c.6864C>T (p.Cys2288=)	rs543264216	0.00001
NM_001267550.2(TTN):c.6855A>C (p.Glu2285Asp)	rs2091955390
NM_001267550.2(TTN):c.7021G>A (p.Asp2341Asn)
NM_001267550.2(TTN):c.7104T>G (p.Cys2368Trp)	rs1485265360
NM_001267550.2(TTN):c.7223A>G (p.Gln2408Arg)	rs777244038

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