ClinVar Miner

List of variants in gene MIB1 reported as likely pathogenic for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_020774.4(MIB1):c.1588C>T (p.Arg530Ter) rs201850378 0.00007
NM_020774.4(MIB1):c.2039del (p.Gln680fs) rs757527279
NM_020774.4(MIB1):c.2878C>T (p.Gln960Ter) rs1430105900

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