List of variants in gene APOB reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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.4838G>C (p.Ser1613Thr)	rs61742247	0.00093
NM_000384.3(APOB):c.914A>G (p.Lys305Arg)	rs199937544	0.00029
NM_000384.3(APOB):c.925G>A (p.Ala309Thr)	rs141888564	0.00026
NM_000384.3(APOB):c.3049A>C (p.Ser1017Arg)	rs149323475	0.00013
NM_000384.3(APOB):c.6655C>T (p.Arg2219Cys)	rs141641980	0.00007
NM_000384.3(APOB):c.6070A>G (p.Ile2024Val)	rs564588440	0.00002
NM_000384.3(APOB):c.11033C>T (p.Pro3678Leu)	rs1278748798	0.00001
NM_000384.3(APOB):c.3404G>A (p.Ser1135Asn)	rs778519921	0.00001
NM_000384.3(APOB):c.10932C>A (p.Phe3644Leu)	rs1572777987
NM_000384.3(APOB):c.11461A>G (p.Thr3821Ala)	rs777808452
NM_000384.3(APOB):c.7520A>G (p.His2507Arg)	rs766283781
NM_000384.3(APOB):c.7529C>T (p.Ala2510Val)	rs1329248076

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