List of variants in gene combination LOC126806425, TTN reported as uncertain significance for TTN-related disorder

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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.53390C>T (p.Thr17797Ile)	rs727503610	0.00001
NM_001267550.2(TTN):c.52531G>A (p.Val17511Ile)	rs1446269783
NM_001267550.2(TTN):c.53011G>T (p.Ala17671Ser)
NM_001267550.2(TTN):c.53122_53123delinsGT (p.Lys17708Val)	rs886042743
NM_001267550.2(TTN):c.53259A>T (p.Lys17753Asn)

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