List of variants in gene combination LOC126806429, 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19976C>T (p.Thr6659Met)	rs16866475	0.01294
NM_001267550.2(TTN):c.20175A>G (p.Ile6725Met)	rs146627500	0.00104
NM_001267550.2(TTN):c.19995A>T (p.Glu6665Asp)	rs146828735	0.00002
NM_001267550.2(TTN):c.20170G>T (p.Val6724Phe)	rs140143513

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