List of variants in gene combination LOC126806430, TTN reported by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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.18824A>G (p.Asn6275Ser)	rs184412722	0.00111
NM_001267550.2(TTN):c.18325A>G (p.Lys6109Glu)	rs73973139	0.00096
NM_001267550.2(TTN):c.18745G>A (p.Asp6249Asn)	rs201263441	0.00021
NM_001267550.2(TTN):c.18628G>A (p.Val6210Ile)	rs766360972	0.00004
NM_001267550.2(TTN):c.18611A>C (p.Glu6204Ala)	rs199603451

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