List of variants in gene APOB reported as pathogenic for not provided

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.10579C>T (p.Arg3527Trp)	rs144467873	0.00006
NM_000384.3(APOB):c.10238del (p.Thr3413fs)	rs756209187	0.00003
NM_000384.3(APOB):c.1315C>T (p.Arg439Ter)	rs142066904	0.00001
NM_000384.3(APOB):c.409G>T (p.Glu137Ter)	rs766243954	0.00001
NM_000384.3(APOB):c.6253C>T (p.Arg2085Ter)	rs121918386	0.00001
NM_000384.3(APOB):c.7600C>T (p.Arg2534Ter)	rs145143533	0.00001
NM_000384.3(APOB):c.10580G>A (p.Arg3527Gln)
NM_000384.3(APOB):c.10848del (p.Gly3617fs)	rs982371659
NM_000384.3(APOB):c.11124del (p.Phe3708fs)	rs1282116285
NM_000384.3(APOB):c.11330C>A (p.Ser3777Ter)
NM_000384.3(APOB):c.2786dup (p.Arg931fs)	rs1553385404
NM_000384.3(APOB):c.3997C>T (p.Arg1333Ter)	rs121918383
NM_000384.3(APOB):c.4832del (p.Phe1611fs)
NM_000384.3(APOB):c.4991del (p.Leu1664fs)	rs2103359058
NM_000384.3(APOB):c.537+1G>T	rs2103384749
NM_000384.3(APOB):c.5564dup (p.Val1856fs)
NM_000384.3(APOB):c.6679del (p.His2227fs)	rs2103356720
NM_000384.3(APOB):c.7961del (p.Asn2654fs)
NM_000384.3(APOB):c.8392G>T (p.Glu2798Ter)	rs923192918

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