List of variants in gene APOB reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.2630C>T (p.Pro877Leu)	rs12714097	0.00063
NM_000384.3(APOB):c.10708C>T (p.His3570Tyr)	rs201736972	0.00021
NM_000384.3(APOB):c.13288T>A (p.Ser4430Thr)	rs72654426	0.00008
NM_000384.3(APOB):c.2312C>T (p.Pro771Leu)	rs200524554	0.00007
NM_000384.3(APOB):c.11929A>C (p.Asn3977His)	rs761528809	0.00001
NM_000384.3(APOB):c.3069G>T (p.Gln1023His)	rs1364541592	0.00001
NM_000384.3(APOB):c.3844G>A (p.Asp1282Asn)	rs781366272	0.00001
NM_000384.3(APOB):c.9794T>C (p.Ile3265Thr)	rs1193351124	0.00001
NM_000384.3(APOB):c.10672C>T (p.Arg3558Cys)
NM_000384.3(APOB):c.12829T>C (p.Ser4277Pro)	rs1663016434
NM_000384.3(APOB):c.1655C>A (p.Ala552Asp)	rs765746519
NM_000384.3(APOB):c.2279A>C (p.Lys760Thr)	rs748468287
NM_000384.3(APOB):c.2870T>A (p.Ile957Asn)	rs2103367360
NM_000384.3(APOB):c.8267G>T (p.Gly2756Val)	rs1663216912

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