List of variants in gene TTN reported as uncertain significance by Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.80701A>G (p.Ile26901Val)	rs201562505	0.00102
NM_001267550.2(TTN):c.87412C>A (p.Pro29138Thr)	rs72648227	0.00073
NM_001267550.2(TTN):c.38902C>T (p.Pro12968Ser)	rs192528655	0.00072
NM_001267550.2(TTN):c.14813T>C (p.Phe4938Ser)	rs560537668	0.00012
NM_001267550.2(TTN):c.57073G>A (p.Val19025Ile)	rs181957743	0.00011
NM_001267550.2(TTN):c.58017G>C (p.Leu19339Phe)	rs368025965	0.00005
NM_001267550.2(TTN):c.3410G>A (p.Gly1137Asp)	rs864309575	0.00001
NM_001267550.2(TTN):c.24229C>A (p.Pro8077Thr)	rs758548104
NM_001267550.2(TTN):c.43978G>A (p.Gly14660Arg)	rs762795774
NM_001267550.2(TTN):c.87616GAA[1] (p.Glu29207del)	rs753636173

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