ClinVar Miner

List of variants in gene combination LOC126806425, TTN reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.53096G>A (p.Arg17699His)	rs72646808	0.00118
NM_001267550.2(TTN):c.53100T>G (p.Pro17700=)	rs373140387	0.00003

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