ClinVar Miner

List of variants in gene combination LOC126806422, TTN reported by Genetics and Genomics Program, Sidra 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.69821G>A (p.Gly23274Asp)	rs201043950	0.00110
NM_001267550.2(TTN):c.70274G>C (p.Ser23425Thr)	rs980974415

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