ClinVar Miner

List of variants reported as likely pathogenic for cardiomyopathy by Institute Of Molecular Biology And Genetics, Federal Almazov National Medical Research Centre

Included ClinVar conditions (522):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_032578.4(MYPN):c.458A>G (p.Lys153Arg) rs199476401 0.00002
NM_001458.5(FLNC):c.3547_3548delinsCT (p.Ala1183Leu) rs1131692185
NM_001458.5(FLNC):c.3557C>T (p.Ala1186Val) rs1114167361
NM_001458.5(FLNC):c.6892C>T (p.Pro2298Ser) rs1554401403
NM_170707.4(LMNA):c.234G>T (p.Lys78Asn) rs727505038
NM_170707.4(LMNA):c.305T>C (p.Leu102Pro) rs1553262007

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