List of variants in gene combination LDLR, MIR6886 reported as likely pathogenic

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.1359-5C>G	rs531005522	0.00004
NM_000527.5(LDLR):c.1474G>C (p.Asp492His)	rs373646964	0.00003
NM_000527.5(LDLR):c.1285G>A (p.Val429Met)	rs28942078	0.00001
NM_000527.5(LDLR):c.1359-1G>A	rs139617694	0.00001
NM_000527.5(LDLR):c.1357_1359-37del	rs1600726930
NM_000527.5(LDLR):c.1359-1G>C	rs139617694
NM_000527.5(LDLR):c.1359-31_1359-23delinsCGGCT	rs879254876

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