ClinVar Miner

List of variants in gene TTN studied for atrial fibrillation (disease)

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_001267550.2(TTN):c.101212C>T (p.Arg33738Cys) rs56273463
NM_001267550.2(TTN):c.18776C>G (p.Thr6259Ser) rs72648949
NM_001267550.2(TTN):c.42513T>A (p.His14171Gln) rs142842339
NM_001267550.2(TTN):c.44014G>A (p.Asp14672Asn) rs1339350914
NM_001267550.2(TTN):c.47315G>A (p.Arg15772Gln) rs72677233
NM_001267550.2(TTN):c.57356A>T (p.Lys19119Met) rs1576219870
NM_001267550.2(TTN):c.57399A>C (p.Leu19133Phe) rs1576219060
NM_001267550.2(TTN):c.63976C>T (p.His21326Tyr) rs1413306492
NM_001267550.2(TTN):c.69130C>T (p.Pro23044Ser) rs55980498
NM_001267550.2(TTN):c.73391G>A (p.Arg24464Gln) rs750056949
NM_001267550.2(TTN):c.87877C>T (p.Arg29293Cys) rs191482653
NM_001267550.2(TTN):c.8902+14T>A rs13388274
NM_001267550.2(TTN):c.9359G>A (p.Arg3120Gln) rs72647894

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