List of variants in gene APOB reported as uncertain significance for digestive system disorder

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000384.3(APOB):c.3843C>T (p.Ser1281=)	rs72653079	0.00240
NM_000384.3(APOB):c.3712C>A (p.Leu1238Ile)	rs72653078	0.00091
NM_000384.3(APOB):c.1470+15T>C	rs185550846	0.00078
NM_000384.3(APOB):c.2853G>A (p.Glu951=)	rs151193347	0.00031
NM_000384.3(APOB):c.10882A>T (p.Asn3628Tyr)	rs141982176	0.00023
NM_000384.3(APOB):c.5763A>G (p.Gly1921=)	rs141022509	0.00023
NM_000384.3(APOB):c.7181T>C (p.Val2394Ala)	rs148429884	0.00023
NM_000384.3(APOB):c.13183G>A (p.Gly4395Ser)	rs151333262	0.00017
NM_000384.3(APOB):c.11466G>A (p.Val3822=)	rs755842633	0.00011
NM_000384.3(APOB):c.11911G>A (p.Glu3971Lys)	rs373477107	0.00009
NM_000384.3(APOB):c.2160C>T (p.Tyr720=)	rs756184175	0.00008
NM_000384.3(APOB):c.4929G>A (p.Ala1643=)	rs200623857	0.00008
NM_000384.3(APOB):c.6656G>A (p.Arg2219His)	rs200106845	0.00008
NM_000384.3(APOB):c.5913G>A (p.Leu1971=)	rs374251542	0.00005
NM_000384.3(APOB):c.2170G>T (p.Gly724Cys)	rs143425834	0.00003
NM_000384.3(APOB):c.2728G>T (p.Gly910Cys)	rs747610107	0.00003
NM_000384.3(APOB):c.7585C>A (p.Gln2529Lys)	rs747140161	0.00003
NM_000384.3(APOB):c.11563A>G (p.Ile3855Val)	rs762255105	0.00001
NM_000384.3(APOB):c.12219C>T (p.Asn4073=)	rs886055573	0.00001
NM_000384.3(APOB):c.12983A>G (p.Tyr4328Cys)	rs886055572	0.00001
NM_000384.3(APOB):c.4216+4A>G	rs886055588	0.00001
NM_000384.3(APOB):c.12088-23dup	rs751121092
NM_000384.3(APOB):c.2917C>A (p.Leu973Met)	rs886055592
NM_000384.3(APOB):c.3595G>A (p.Asp1199Asn)	rs375894411
NM_000384.3(APOB):c.7405T>A (p.Phe2469Ile)	rs768221258

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