List of variants in gene combination LOC126806421, TTN reported as uncertain significance for Cardiomyopathy

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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.96424G>A (p.Val32142Ile)	rs779663332	0.00006
NM_001267550.2(TTN):c.96235G>C (p.Asp32079His)	rs200540781
NM_001267550.2(TTN):c.96289A>G (p.Thr32097Ala)	rs1559126718
NM_001267550.2(TTN):c.96593T>C (p.Leu32198Pro)	rs2154143465
NM_001267550.2(TTN):c.96812A>G (p.Glu32271Gly)	rs1559120065

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