ClinVar Miner

List of variants in gene TTN reported by Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin

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.13807del (p.Glu4603fs)	rs1574066113
NM_001267550.2(TTN):c.2073A>T (p.Gly691=)	rs72647860
NM_001267550.2(TTN):c.31846+1G>A	rs794727043

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