List of variants in gene combination LOC126806430, TTN reported as benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18903C>T (p.Thr6301=)	rs72648950	0.01956
NM_001267550.2(TTN):c.18776C>G (p.Thr6259Ser)	rs72648949	0.00262
NM_001267550.2(TTN):c.18856G>A (p.Val6286Ile)	rs149131555	0.00184
NM_001267550.2(TTN):c.18961A>G (p.Ile6321Val)	rs145204073	0.00146
NM_001267550.2(TTN):c.18824A>G (p.Asn6275Ser)	rs184412722	0.00111
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18172C>T (p.Arg6058Cys)	rs189127014	0.00053
NM_001267550.2(TTN):c.18745G>A (p.Asp6249Asn)	rs201263441	0.00021
NM_001267550.2(TTN):c.18816T>C (p.Ile6272=)	rs146219199	0.00012
NM_001267550.2(TTN):c.18379T>G (p.Cys6127Gly)	rs370812788	0.00011

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