List of variants in gene combination LOC126806421, TTN reported as benign for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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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
NM_001267550.2(TTN):c.96918C>T (p.Ile32306=)	rs72648266	0.00064
NM_001267550.2(TTN):c.96904+8C>T	rs528358945	0.00001
NM_001267550.2(TTN):c.96180T>C (p.Ile32060=)	rs572401798

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