ClinVar Miner

List of variants in gene combination LOC126806425, TTN reported by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.52702A>G (p.Ile17568Val)	rs377571654	0.00011
NM_001267550.2(TTN):c.52515G>A (p.Trp17505Ter)	rs1160660090

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