ClinVar Miner

List of variants in gene combination LOC126806422, TTN reported by Cardiovascular Biomedical Research Unit, Royal Brompton & Harefield NHS Foundation Trust

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69630C>A (p.Tyr23210Ter)	rs777602537
NM_001267550.2(TTN):c.69843del (p.Lys23281_Val23282insTer)	rs869312075
NM_001267550.2(TTN):c.69877G>T (p.Gly23293Ter)	rs869312114

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