List of variants in gene combination ABHD12, LOC130065586 reported as benign for syndromic dyslipidemia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001042472.2(ABHD12):c.-220G>A	rs3827014	0.54397
NM_001042472.3(ABHD12):c.-94C>T	rs536190889	0.02252
NM_001042472.3(ABHD12):c.-40_-39insGGCGGAGGC	rs3833297

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