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

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.1359-1G>A	rs139617694	0.00001
NC_000019.10:g.(?_11100213)_(11117013_?)del
NC_000019.10:g.(?_11111494)_(11113782_?)del
NC_000019.10:g.(?_11111504)_(11117013_?)del
NC_000019.10:g.(?_11113272)_(11120528_?)del
NM_000527.5(LDLR):c.1359-1G>C	rs139617694

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