List of variants in gene combination LOC126806425, TTN reported as benign by Clinical Genetics, Academic Medical Center

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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.52917T>C (p.Asp17639=)	rs73036398	0.02352
NM_001267550.2(TTN):c.52821T>C (p.Asp17607=)	rs2303831	0.02082
NM_001267550.2(TTN):c.53123A>T (p.Lys17708Ile)	rs2303832	0.02072
NM_001267550.2(TTN):c.52706-17A>G	rs72646807	0.01524
NM_001267550.2(TTN):c.53192T>C (p.Ile17731Thr)	rs72646809	0.01131
NM_001267550.2(TTN):c.53288-18G>T	rs72646810	0.00643
NM_001267550.2(TTN):c.52852C>T (p.Arg17618Cys)	rs201213901	0.00115
NM_001267550.2(TTN):c.52536C>G (p.Asn17512Lys)	rs199615557	0.00034
NM_001267550.2(TTN):c.53260T>C (p.Phe17754Leu)	rs397517612	0.00001

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