List of variants in gene combination LOC126806421, TTN reported as benign for Cardiovascular phenotype

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96158T>C (p.Ile32053Thr)	rs62621236	0.08189
NM_001267550.2(TTN):c.96944C>T (p.Thr32315Ile)	rs56027402	0.01724
NM_001267550.2(TTN):c.96501T>C (p.Ser32167=)	rs139223781	0.00251
NM_001267550.2(TTN):c.96108G>A (p.Val32036=)	rs372773283	0.00234

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