List of variants in gene combination LOC126806430, TTN reported by Athena Diagnostics

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: 10

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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.18824A>G (p.Asn6275Ser)	rs184412722	0.00111
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18531G>C (p.Val6177=)	rs370684491	0.00088
NM_001267550.2(TTN):c.18379T>G (p.Cys6127Gly)	rs370812788	0.00011
NM_001267550.2(TTN):c.18663A>C (p.Glu6221Asp)	rs369544339	0.00010
NM_001267550.2(TTN):c.18775A>G (p.Thr6259Ala)	rs780049500	0.00010
NM_001267550.2(TTN):c.18655G>A (p.Glu6219Lys)	rs72648948	0.00004
NM_001267550.2(TTN):c.18719G>A (p.Arg6240Gln)	rs761993856	0.00004
NM_001267550.2(TTN):c.18589G>C (p.Glu6197Gln)	rs753281535	0.00001

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