ClinVar Miner

List of variants in gene LDLRAP1 reported as benign for Hypercholesterolemia, familial, 1

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_015627.3(LDLRAP1):c.985_986insTG	rs10635955	0.99254
NM_015627.3(LDLRAP1):c.*449del	rs397860393

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