ClinVar Miner

List of variants in gene combination LDLRAP1, LOC129929773 reported as uncertain significance for Familial hypercholesterolemia

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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.78C>T (p.Gly26=)	rs928922661	0.00021
NM_015627.3(LDLRAP1):c.34A>G (p.Ile12Val)	rs1250534468	0.00001

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