List of variants in gene combination LOC126806420, 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.99901G>A (p.Glu33301Lys)	rs72648278	0.00041
NM_001267550.2(TTN):c.99991T>C (p.Cys33331Arg)	rs56061641	0.00022
NM_001267550.2(TTN):c.100226G>A (p.Cys33409Tyr)	rs201112096	0.00011
NM_001267550.2(TTN):c.100315T>C (p.Trp33439Arg)	rs545443009	0.00006
NM_001267550.2(TTN):c.99900C>T (p.Ile33300=)	rs747130957	0.00001
NM_001267550.2(TTN):c.99966G>T (p.Trp33322Cys)	rs775769503

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