List of variants in gene combination LOC126806422, TTN reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.70492G>A (p.Gly23498Ser)	rs370771532	0.00026
NM_001267550.2(TTN):c.70102A>G (p.Ile23368Val)	rs367914610	0.00005
NM_001267550.2(TTN):c.70328G>A (p.Arg23443Gln)	rs762529671	0.00004
NM_001267550.2(TTN):c.69815T>G (p.Ile23272Ser)	rs758398301	0.00001
NM_001267550.2(TTN):c.70013G>A (p.Arg23338Gln)	rs78916558	0.00001
NM_001267550.2(TTN):c.69716-15T>C
NM_001267550.2(TTN):c.70082G>T (p.Ser23361Ile)	rs1433418101
NM_001267550.2(TTN):c.70343C>A (p.Thr23448Lys)
NM_001267550.2(TTN):c.70379T>G (p.Leu23460Arg)

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