List of variants in gene combination FBXO11, LOC100506235 reported as uncertain significance for Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001190274.2(FBXO11):c.107C>T (p.Pro36Leu)	rs1412913967
NM_001190274.2(FBXO11):c.125A>G (p.Gln42Arg)	rs975859124
NM_001190274.2(FBXO11):c.134_157del (p.Pro45_Gln52del)	rs1371955576
NM_001190274.2(FBXO11):c.149A>G (p.Gln50Arg)	rs781277953
NM_001190274.2(FBXO11):c.166C>T (p.Gln56Ter)
NM_001190274.2(FBXO11):c.84dup (p.Gln29fs)	rs2104141116

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