ClinVar Miner

List of variants in gene combination LOC129935185, TTN reported by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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.105180G>C (p.Glu35060Asp)	rs56308529	0.03418
NM_001267550.2(TTN):c.105136G>A (p.Glu35046Lys)	rs540500017

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