ClinVar Miner

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

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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NM_001365068.1(ASTN2):c.2806+24861A>G rs2281627
NM_001365068.1(ASTN2):c.2806+25478C>T rs16933835
NM_001365068.1(ASTN2):c.2806+25938G>A rs3019
NM_001365068.1(ASTN2):c.2806+26775C>T rs1661300
NM_001365068.1(ASTN2):c.2806+27259G>C rs3747834
NM_001365068.1(ASTN2):c.2806+28023A>C rs141352486
NM_001365068.1(ASTN2):c.2807-35537C>G rs12342207

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