List of variants in gene combination LOC126806421, 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96172C>T (p.Arg32058Trp)	rs201463708	0.00008
NM_001267550.2(TTN):c.96637G>A (p.Asp32213Asn)	rs764561909	0.00006
NM_001267550.2(TTN):c.96434G>A (p.Arg32145His)	rs759948951	0.00003
NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser)	rs1024823449	0.00003
NM_001267550.2(TTN):c.96745T>C (p.Trp32249Arg)	rs370515456	0.00002
NM_001267550.2(TTN):c.96054T>G (p.Asp32018Glu)	rs773714477	0.00001
NM_001267550.2(TTN):c.96159T>G (p.Ile32053Met)	rs906167122	0.00001
NM_001267550.2(TTN):c.96428A>G (p.Glu32143Gly)	rs904892183	0.00001

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