ClinVar Miner

List of variants in gene MAFB reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_005461.5(MAFB):c.*1019A>G rs545693248
NM_005461.5(MAFB):c.*1210G>A rs542788257
NM_005461.5(MAFB):c.*1255C>T rs573637366
NM_005461.5(MAFB):c.*1314A>G rs533750110
NM_005461.5(MAFB):c.*1519C>G rs185930615
NM_005461.5(MAFB):c.*1520C>G rs148352161
NM_005461.5(MAFB):c.*152G>C rs553723079
NM_005461.5(MAFB):c.*155C>T rs533850442
NM_005461.5(MAFB):c.*1737A>G rs532037681
NM_005461.5(MAFB):c.*503_*506TGTC[1] rs201579991
NM_005461.5(MAFB):c.*68G>A rs190300765
NM_005461.5(MAFB):c.-204_-203del rs201369817
NM_005461.5(MAFB):c.-206T>G rs527524576
NM_005461.5(MAFB):c.-310G>A rs567415398
NM_005461.5(MAFB):c.-75C>G rs574807151
NM_005461.5(MAFB):c.253C>A (p.Leu85Met) rs377639854
NM_005461.5(MAFB):c.745C>A (p.Arg249=) rs561320614

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