List of variants in gene combination LOC126806430, TTN reported by Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18776C>G (p.Thr6259Ser)	rs72648949	0.00262
NM_001267550.2(TTN):c.18856G>A (p.Val6286Ile)	rs149131555	0.00184
NM_001267550.2(TTN):c.18961A>G (p.Ile6321Val)	rs145204073	0.00146
NM_001267550.2(TTN):c.18824A>G (p.Asn6275Ser)	rs184412722	0.00111
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18550G>A (p.Ala6184Thr)	rs72648947	0.00046

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