ClinVar Miner

List of variants reported as benign for autosomal recessive limb-girdle muscular dystrophy type 2H

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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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.2807-35537C>G rs12342207
NM_012210.4(TRIM32):c.1254G>A (p.Val418=) rs1661300

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