List of variants in gene APOB reported as likely pathogenic by Invitae

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.2604+1G>A	rs775345377	0.00002
NM_000384.3(APOB):c.1618-2A>C	rs373251374	0.00001
NC_000002.11:g.(?_21229172)_(21237720_?)del
NM_000384.3(APOB):c.10181A>C (p.Lys3394Thr)	rs1663150812
NM_000384.3(APOB):c.11789-1G>C	rs1558560212
NM_000384.3(APOB):c.1470+2T>C
NM_000384.3(APOB):c.3508+1G>A	rs867418897
NM_000384.3(APOB):c.3508+1G>T	rs867418897
NM_000384.3(APOB):c.693+2T>A	rs2103383976
NM_000384.3(APOB):c.694-4_694-2del
NM_000384.3(APOB):c.819-2A>G	rs1572800245
NM_000384.3(APOB):c.904+1G>A

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