List of variants in gene combination LDLR, MIR6886 reported as likely benign 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)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.1359-31G>A	rs369781605	0.00006
NM_000527.5(LDLR):c.1359-3C>T	rs775657243	0.00006
NM_000527.5(LDLR):c.1359-10C>T	rs779530380	0.00001
NM_000527.5(LDLR):c.1359-13C>T	rs886038307	0.00001
NM_000527.5(LDLR):c.1359-29G>A	rs879254877	0.00001
NM_000527.5(LDLR):c.1359-13C>A
NM_000527.5(LDLR):c.1359-14T>G	rs2077413900
NM_000527.5(LDLR):c.1359-20C>T
NM_000527.5(LDLR):c.1359-26G>A	rs2077413668
NM_000527.5(LDLR):c.1359-29G>C
NM_000527.5(LDLR):c.1359-5C>T	rs531005522
NM_000527.5(LDLR):c.1359-6C>A
NM_000527.5(LDLR):c.1359-6C>T

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