List of variants in gene APOB studied for Hypobetalipoproteinemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.10238del (p.Thr3413fs)	rs756209187	0.00003
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.11812_11813del (p.Asp3938fs)	rs1553382678
NM_000384.3(APOB):c.13025del (p.Pro4342fs)	rs797045253
NM_000384.3(APOB):c.2988_2994del (p.Gly997fs)	rs1057518647
NM_000384.3(APOB):c.3778G>T (p.Glu1260Ter)	rs144892654
NM_000384.3(APOB):c.4139_4140del (p.Thr1380fs)
NM_000384.3(APOB):c.631C>T (p.Gln211Ter)	rs143301836
NM_000384.3(APOB):c.8739_8740del (p.Leu2914fs)
NM_000384.3(APOB):c.8898dup (p.His2967fs)

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