ClinVar Miner

List of variants in gene combination LOC126806422, TTN reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 25
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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.69676A>G (p.Ser23226Gly) rs72646885 0.00553
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.70491C>T (p.Thr23497=) rs372382315 0.00031
NM_001267550.2(TTN):c.69864A>G (p.Ile23288Met) rs368867993 0.00026
NM_001267550.2(TTN):c.70492G>A (p.Gly23498Ser) rs370771532 0.00026
NM_001267550.2(TTN):c.70131A>G (p.Thr23377=) rs369503828 0.00010
NM_001267550.2(TTN):c.70042G>A (p.Ala23348Thr) rs775146212 0.00007
NM_001267550.2(TTN):c.70102A>G (p.Ile23368Val) rs367914610 0.00005
NM_001267550.2(TTN):c.70328G>A (p.Arg23443Gln) rs762529671 0.00004
NM_001267550.2(TTN):c.69828C>T (p.Val23276=) rs55659506 0.00002
NM_001267550.2(TTN):c.69960C>T (p.Asn23320=) rs752969136 0.00002
NM_001267550.2(TTN):c.69815T>G (p.Ile23272Ser) rs758398301 0.00001
NM_001267550.2(TTN):c.70013G>A (p.Arg23338Gln) rs78916558 0.00001
NM_001267550.2(TTN):c.69716-15T>C
NM_001267550.2(TTN):c.69838C>T (p.Gln23280Ter) rs1710057805
NM_001267550.2(TTN):c.69888C>G (p.Leu23296=) rs2154172842
NM_001267550.2(TTN):c.70082G>T (p.Ser23361Ile) rs1433418101
NM_001267550.2(TTN):c.70203T>C (p.Ile23401=) rs2154172628
NM_001267550.2(TTN):c.70343C>A (p.Thr23448Lys)
NM_001267550.2(TTN):c.70379T>G (p.Leu23460Arg)
NM_001267550.2(TTN):c.70623C>A (p.Ile23541=)

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