ClinVar Miner

List of variants in gene combination ASTN2, TRIM32 reported as likely benign for Bardet-Biedl syndrome

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Total variants: 17
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HGVS dbSNP
NM_001365068.1(ASTN2):c.2806+26079A>G rs1273018123
NM_001365068.1(ASTN2):c.2806+26367A>G rs372044621
NM_001365068.1(ASTN2):c.2806+26643C>T rs762905941
NM_001365068.1(ASTN2):c.2806+26703A>T rs1372713940
NM_001365068.1(ASTN2):c.2806+26807G>A rs3747835
NM_001365068.1(ASTN2):c.2806+26889G>A rs142715198
NM_001365068.1(ASTN2):c.2806+27222C>T rs1184553729
NM_001365068.1(ASTN2):c.2806+27234G>C rs756049046
NM_001365068.1(ASTN2):c.2806+27351G>A rs398124253
NM_001365068.1(ASTN2):c.2806+27369C>G rs3747833
NM_001365068.1(ASTN2):c.2806+27471C>G rs117599771
NM_001365068.1(ASTN2):c.2806+27528C>T rs200085883
NM_001365068.1(ASTN2):c.2806+27620G>A rs200997003
NM_001365068.1(ASTN2):c.2806+27663G>C rs137947083
NM_001365068.1(ASTN2):c.2806+27753G>A rs140589523
NM_001365068.1(ASTN2):c.2806+27828A>G rs780799984
NM_001365068.1(ASTN2):c.2806+28002C>G rs201891227

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