List of variants in gene combination LOC126806421, TTN reported as uncertain significance by Athena Diagnostics

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96173G>A (p.Arg32058Gln)	rs374063064	0.00014
NM_001267550.2(TTN):c.96526T>A (p.Tyr32176Asn)	rs377291343	0.00006
NM_001267550.2(TTN):c.96551T>C (p.Ile32184Thr)	rs952755219	0.00001
NM_001267550.2(TTN):c.96872C>T (p.Thr32291Ile)	rs780461366	0.00001
NM_001267550.2(TTN):c.96082G>A (p.Ala32028Thr)

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