List of variants in gene combination LOC126806423, 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.68161G>A (p.Glu22721Lys)	rs374492812	0.00011
NM_001267550.2(TTN):c.67444C>T (p.Arg22482Trp)	rs563233842	0.00002
NM_001267550.2(TTN):c.68078C>T (p.Thr22693Met)	rs758700425	0.00001
NM_001267550.2(TTN):c.68065A>G (p.Asn22689Asp)	rs786205382

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