ClinVar Miner

List of variants in gene combination LDB3, LOC110121486 reported as likely benign for autosomal dominant distal myopathy

Included ClinVar conditions (33):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_007078.3(LDB3):c.690-4661G>A rs373632943
NM_007078.3(LDB3):c.690-4668T>C rs76615432
NM_007078.3(LDB3):c.690-4704G>A rs745413406
NM_007078.3(LDB3):c.690-4707C>T rs200462775
NM_007078.3(LDB3):c.690-4719T>C
NM_007078.3(LDB3):c.690-4740C>T
NM_007078.3(LDB3):c.690-4757G>A rs374613600
NM_007078.3(LDB3):c.690-4758C>T rs372423575
NM_007078.3(LDB3):c.690-4779C>T
NM_007078.3(LDB3):c.690-4803C>T rs751576160
NM_007078.3(LDB3):c.690-4824C>T rs397516557
NM_007078.3(LDB3):c.690-4835T>A
NM_007078.3(LDB3):c.690-4842G>A rs113445294

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