ClinVar Miner

List of variants in gene combination LOC126806429, TTN reported by Mayo Clinic Laboratories, Mayo Clinic

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.20057G>A (p.Arg6686Gln)	rs202022304	0.00004
NM_001267550.2(TTN):c.20125C>T (p.Pro6709Ser)
NM_001267550.2(TTN):c.20185A>C (p.Asn6729His)	rs794729619

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