List of variants in gene LDLRAP1 reported as benign for Familial hypercholesterolemia

Minimum submission review status:		Collection method:
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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_015627.3(LDLRAP1):c.654A>G (p.Thr218=)	rs28969504	0.62316
NM_015627.3(LDLRAP1):c.604T>C (p.Ser202Pro)	rs6687605	0.47789
NM_015627.3(LDLRAP1):c.712C>T (p.Arg238Trp)	rs41291058	0.03285

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