ClinVar Miner

List of variants in gene combination LOC126806433, TTN reported as benign for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J

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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.7174G>A (p.Gly2392Ser)	rs4894048	0.05739
NM_001267550.2(TTN):c.7061G>A (p.Arg2354His)	rs75031300	0.00287

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