List of variants in gene combination LOC126806427, 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.45408G>T (p.Lys15136Asn)	rs72677225	0.00512
NM_001267550.2(TTN):c.45599C>G (p.Ala15200Gly)	rs201057307	0.00030
NM_001267550.2(TTN):c.45273C>T (p.Asn15091=)	rs72677223	0.00026
NM_001267550.2(TTN):c.45212T>C (p.Ile15071Thr)	rs184078045	0.00006
NM_001267550.2(TTN):c.45054G>A (p.Ala15018=)	rs781392140	0.00003
NM_001267550.2(TTN):c.44999T>C (p.Ile15000Thr)	rs886055275

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