List of variants in gene combination LOC126806429, TTN reported as uncertain significance for Dilated cardiomyopathy 1G

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19738C>T (p.Pro6580Ser)	rs116572520	0.00188
NM_001267550.2(TTN):c.20108G>A (p.Arg6703Gln)	rs546821182	0.00014
NM_001267550.2(TTN):c.19770A>G (p.Thr6590=)	rs775289296	0.00004
NM_001267550.2(TTN):c.19995A>T (p.Glu6665Asp)	rs146828735	0.00002
NM_001267550.2(TTN):c.19994-13C>T	rs775393005	0.00001

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