List of variants in gene APC2 reported as uncertain significance for autosomal recessive non-syndromic intellectual disability

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_005883.3(APC2):c.5108C>A (p.Ala1703Glu)	rs200444154	0.00100
NM_005883.3(APC2):c.3656C>T (p.Ala1219Val)	rs137877386	0.00093
NM_005883.3(APC2):c.3979C>T (p.Pro1327Ser)	rs535779056	0.00092
NM_005883.3(APC2):c.1778C>T (p.Ser593Leu)	rs750829429	0.00005
NM_005883.3(APC2):c.1628G>A (p.Arg543Gln)
NM_005883.3(APC2):c.2372C>T (p.Ala791Val)
NM_005883.3(APC2):c.2518_2523dup (p.Ala841_Lys842insAlaAla)
NM_005883.3(APC2):c.2595C>A (p.His865Gln)	rs2145233148
NM_005883.3(APC2):c.2651C>A (p.Pro884Gln)
NM_005883.3(APC2):c.2686C>G (p.Arg896Gly)
NM_005883.3(APC2):c.3019G>A (p.Gly1007Ser)
NM_005883.3(APC2):c.4603C>T (p.Arg1535Cys)
NM_005883.3(APC2):c.4616G>C (p.Arg1539Pro)	rs367655515
NM_005883.3(APC2):c.5123G>T (p.Arg1708Leu)
NM_005883.3(APC2):c.583C>T (p.Arg195Cys)	rs1158412843
NM_005883.3(APC2):c.6111C>T (p.Phe2037=)	rs1405418055
NM_005883.3(APC2):c.757C>T (p.Pro253Ser)	rs555858661
NM_005883.3(APC2):c.796C>A (p.Pro266Thr)	rs146579468

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