ClinVar Miner

List of variants in gene combination HADH, LOC129992931 reported as benign by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005327.4(HADH):c.-65G>A	rs28703310	0.01115
NM_005327.4(HADH):c.-56C>A	rs770197760

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