List of variants in gene combination LOC126806428, TTN reported as benign for autosomal recessive disease

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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.20861C>T (p.Ala6954Val)	rs17355446	0.02915
NM_001267550.2(TTN):c.21106G>A (p.Asp7036Asn)	rs72648962	0.01709
NM_001267550.2(TTN):c.21044C>T (p.Ala7015Val)	rs72648960	0.00666
NM_001267550.2(TTN):c.21019A>T (p.Ile7007Phe)	rs114626713	0.00491
NM_001267550.2(TTN):c.21173G>A (p.Gly7058Asp)	rs72648964	0.00354
NM_001267550.2(TTN):c.20874G>A (p.Thr6958=)	rs765956215	0.00004

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