ClinVar Miner

List of variants in gene combination LDLRAP1, LOC129929773 reported as likely benign for Familial hypercholesterolemia

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.75T>A (p.Gly25=)	rs1057515462	0.00005
NM_015627.3(LDLRAP1):c.27G>A (p.Arg9=)	rs1340216590

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