List of variants in gene combination LOC126806423, 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.68097G>C (p.Gln22699His)	rs727504520	0.00008
NM_001267550.2(TTN):c.67496G>A (p.Arg22499Gln)	rs767993624	0.00002
NM_001267550.2(TTN):c.67960G>C (p.Asp22654His)	rs144295295	0.00001
NM_001267550.2(TTN):c.68300C>T (p.Pro22767Leu)	rs775953148	0.00001
NM_001267550.2(TTN):c.67565G>C (p.Arg22522Thr)	rs1221271318

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