List of variants in gene combination LOC126806431, TTN reported as benign for Early-onset myopathy with fatal cardiomyopathy

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.17312C>G (p.Thr5771Ser)	rs16866477	0.00593
NM_001267550.2(TTN):c.17300G>A (p.Ser5767Asn)	rs200692495	0.00103
NM_001267550.2(TTN):c.17115C>T (p.Gly5705=)	rs370036981	0.00058
NM_001267550.2(TTN):c.17319C>T (p.Asp5773=)	rs760724229	0.00002

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