List of variants in gene combination LOC126806423, 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67604G>A (p.Ser22535Asn)	rs375676529	0.00012
NM_001267550.2(TTN):c.67487A>G (p.Lys22496Arg)	rs397517669	0.00002
NM_001267550.2(TTN):c.68195C>T (p.Ser22732Leu)	rs727505352	0.00001
NM_001267550.2(TTN):c.67781A>T (p.Asp22594Val)
NM_001267550.2(TTN):c.68314G>C (p.Gly22772Arg)	rs1559480997

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