List of variants in gene combination LOC126806422, 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69585C>T (p.Ser23195=)	rs67041405	0.01183
NM_001267550.2(TTN):c.69740C>T (p.Pro23247Leu)	rs115658240	0.00835
NM_001267550.2(TTN):c.69716-5C>G	rs72646886	0.00290
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp)	rs201043950	0.00110
NM_001267550.2(TTN):c.70250T>C (p.Ile23417Thr)	rs201836227	0.00086
NM_001267550.2(TTN):c.70131A>G (p.Thr23377=)	rs369503828	0.00010
NM_001267550.2(TTN):c.70506G>T (p.Gly23502=)	rs181702963	0.00007
NM_001267550.2(TTN):c.70305G>A (p.Thr23435=)	rs397517684	0.00006
NM_001267550.2(TTN):c.70036C>T (p.Leu23346=)	rs397517681	0.00004
NM_001267550.2(TTN):c.70288G>A (p.Val23430Ile)	rs549709481	0.00004
NM_001267550.2(TTN):c.70485A>T (p.Lys23495Asn)	rs1482776876	0.00002
NM_001267550.2(TTN):c.69959A>G (p.Asn23320Ser)	rs756468956	0.00001
NM_001267550.2(TTN):c.70181C>T (p.Thr23394Met)	rs397517683	0.00001
NM_001267550.2(TTN):c.69841_69843dup (p.Lys23281dup)	rs869312075
NM_001267550.2(TTN):c.69903C>A (p.Phe23301Leu)	rs372799151

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