List of variants in gene combination LOC126806423, TTN reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67606G>A (p.Glu22536Lys)	rs371105318	0.00006
NM_001267550.2(TTN):c.67726G>A (p.Gly22576Ser)
NM_001267550.2(TTN):c.68059G>T (p.Val22687Leu)
NM_001267550.2(TTN):c.68144C>A (p.Thr22715Asn)

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