List of variants in gene combination LOC126806430, TTN reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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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.18550G>A (p.Ala6184Thr)	rs72648947	0.00046
NM_001267550.2(TTN):c.18745G>A (p.Asp6249Asn)	rs201263441	0.00021
NM_001267550.2(TTN):c.18816T>C (p.Ile6272=)	rs146219199	0.00012
NM_001267550.2(TTN):c.18561G>A (p.Ala6187=)	rs377556808	0.00004
NM_001267550.2(TTN):c.18681G>A (p.Pro6227=)	rs372273496	0.00004
NM_001267550.2(TTN):c.18645C>T (p.Asp6215=)	rs372400829	0.00003
NM_001267550.2(TTN):c.18589+4C>T	rs1449021840	0.00001
NM_001267550.2(TTN):c.18276A>G (p.Thr6092=)	rs751657803
NM_001267550.2(TTN):c.18552A>G (p.Ala6184=)
NM_001267550.2(TTN):c.18732A>G (p.Lys6244=)

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