ClinVar Miner

List of variants reported as likely benign for autosomal dominant distal myopathy by Centre for Mendelian Genomics,University Medical Centre Ljubljana

Included ClinVar conditions (33):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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NM_001267550.2(TTN):c.26672A>G (p.Asn8891Ser) rs146057575
NM_001267550.2(TTN):c.29230C>T (p.Arg9744Cys) rs375266859
NM_001267550.2(TTN):c.33053G>A (p.Arg11018Gln) rs72650034
NM_001267550.2(TTN):c.3988C>T (p.Arg1330Cys) rs771294359
NM_001267550.2(TTN):c.42329T>C (p.Val14110Ala) rs34706299

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