ClinVar Miner

List of variants in gene combination LOC126806421, TTN reported as likely benign for Cardiovascular phenotype

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.96098G>A (p.Arg32033His) rs200648462 0.00090
NM_001267550.2(TTN):c.96918C>T (p.Ile32306=) rs72648266 0.00064
NM_001267550.2(TTN):c.96234C>T (p.Tyr32078=) rs376532382 0.00018
NM_001267550.2(TTN):c.96252A>G (p.Thr32084=) rs369626133 0.00018
NM_001267550.2(TTN):c.96138A>T (p.Ile32046=) rs368154623 0.00016
NM_001267550.2(TTN):c.96684C>T (p.Tyr32228=) rs368423941 0.00016
NM_001267550.2(TTN):c.96904+4T>C rs373514079 0.00014
NM_001267550.2(TTN):c.96051A>G (p.Ala32017=) rs367805587 0.00008
NM_001267550.2(TTN):c.96873T>C (p.Thr32291=) rs368169892 0.00007
NM_001267550.2(TTN):c.96286G>A (p.Ala32096Thr) rs376039623 0.00005
NM_001267550.2(TTN):c.96189C>T (p.Thr32063=) rs544886477 0.00004
NM_001267550.2(TTN):c.96225T>A (p.Val32075=) rs752745266 0.00004
NM_001267550.2(TTN):c.96390G>A (p.Thr32130=) rs200999706 0.00004
NM_001267550.2(TTN):c.96384T>C (p.Ile32128=) rs757368075 0.00003
NM_001267550.2(TTN):c.96525C>T (p.Tyr32175=) rs778126823 0.00003
NM_001267550.2(TTN):c.96708A>G (p.Gly32236=) rs752066259 0.00003
NM_001267550.2(TTN):c.96906G>A (p.Val32302=) rs200276343 0.00003
NM_001267550.2(TTN):c.96921T>C (p.Asp32307=) rs771385738 0.00003
NM_001267550.2(TTN):c.96420C>T (p.Tyr32140=) rs1009407656 0.00002
NM_001267550.2(TTN):c.96336G>T (p.Val32112=) rs964067201 0.00001
NM_001267550.2(TTN):c.96615G>A (p.Val32205=) rs763674509 0.00001
NM_001267550.2(TTN):c.96717C>T (p.Leu32239=) rs1317384618 0.00001
NM_001267550.2(TTN):c.96834G>A (p.Arg32278=) rs558927011 0.00001
NM_001267550.2(TTN):c.96837A>C (p.Ala32279=) rs1232489828 0.00001
NM_001267550.2(TTN):c.96048T>C (p.Leu32016=)
NM_001267550.2(TTN):c.96075C>T (p.Thr32025=)
NM_001267550.2(TTN):c.96090C>T (p.Ala32030=) rs1575420522
NM_001267550.2(TTN):c.96141G>A (p.Thr32047=) rs752553035
NM_001267550.2(TTN):c.96153G>A (p.Gln32051=)
NM_001267550.2(TTN):c.96180T>C (p.Ile32060=) rs572401798
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn) rs200540781
NM_001267550.2(TTN):c.96294C>T (p.Val32098=)
NM_001267550.2(TTN):c.96297T>C (p.Leu32099=)
NM_001267550.2(TTN):c.96411C>G (p.Val32137=) rs1329249610
NM_001267550.2(TTN):c.96442G>A (p.Ala32148Thr)
NM_001267550.2(TTN):c.96534A>G (p.Arg32178=)
NM_001267550.2(TTN):c.96538C>T (p.Leu32180=)
NM_001267550.2(TTN):c.96555T>C (p.Tyr32185=) rs1575412584
NM_001267550.2(TTN):c.96570T>C (p.Pro32190=) rs1223460802
NM_001267550.2(TTN):c.96585T>C (p.Asp32195=)
NM_001267550.2(TTN):c.96588A>G (p.Ala32196=)
NM_001267550.2(TTN):c.96591A>T (p.Val32197=)
NM_001267550.2(TTN):c.96610T>C (p.Leu32204=) rs1419384451
NM_001267550.2(TTN):c.96621A>G (p.Ala32207=)
NM_001267550.2(TTN):c.96636C>T (p.Val32212=)
NM_001267550.2(TTN):c.96708A>C (p.Gly32236=)
NM_001267550.2(TTN):c.96711T>C (p.Tyr32237=)
NM_001267550.2(TTN):c.96735C>T (p.Gly32245=)
NM_001267550.2(TTN):c.96738A>T (p.Thr32246=)
NM_001267550.2(TTN):c.96789T>C (p.Thr32263=)
NM_001267550.2(TTN):c.96804T>C (p.Asn32268=)
NM_001267550.2(TTN):c.96816A>G (p.Gln32272=) rs2154143321
NM_001267550.2(TTN):c.96819C>T (p.Tyr32273=)
NM_001267550.2(TTN):c.96843T>C (p.Asn32281=)
NM_001267550.2(TTN):c.96852T>C (p.Gly32284=)
NM_001267550.2(TTN):c.96858A>G (p.Ser32286=) rs1035330963
NM_001267550.2(TTN):c.96879A>C (p.Thr32293=) rs373707659
NM_001267550.2(TTN):c.96879A>G (p.Thr32293=) rs373707659

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