List of variants in gene combination LOC126806421, 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96286G>A (p.Ala32096Thr)	rs376039623	0.00005
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn)	rs200540781
NM_001267550.2(TTN):c.96586G>A (p.Ala32196Thr)

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