List of variants in gene APOE studied for syndromic dyslipidemia

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000041.4(APOE):c.388T>C (p.Cys130Arg)	rs429358	0.16059
NM_000041.4(APOE):c.651C>T (p.Ala217=)	rs72654468	0.00090
NM_000041.4(APOE):c.91G>A (p.Glu31Lys)	rs201672011	0.00049
NM_000041.4(APOE):c.805C>G (p.Arg269Gly)	rs267606661	0.00032
NM_000041.4(APOE):c.69G>A (p.Ala23=)	rs111833428	0.00024
NM_000041.4(APOE):c.434G>A (p.Gly145Asp)	rs267606664	0.00013
NM_000041.4(APOE):c.249C>T (p.Asp83=)	rs767980905	0.00003
NM_000041.4(APOE):c.688G>A (p.Glu230Lys)	rs567353589	0.00002
NM_000041.4(APOE):c.127C>T (p.Arg43Cys)	rs121918399	0.00001
NM_000041.4(APOE):c.488G>A (p.Arg163His)	rs121918397	0.00001
NM_000041.4(APOE):c.31A>G (p.Thr11Ala)
NM_000041.4(APOE):c.488G>C (p.Arg163Pro)	rs121918397
NM_000041.4(APOE):c.488G>T (p.Arg163Leu)	rs121918397
NM_000041.4(APOE):c.494G>C (p.Arg165Pro)	rs1332591068
NM_000041.4(APOE):c.497TCC[1] (p.Leu167del)	rs515726148

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