List of variants in gene TRAPPC9 reported as uncertain significance for 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001160372.4(TRAPPC9):c.3149G>A (p.Arg1050Gln)	rs111768745	0.00098
NM_001160372.4(TRAPPC9):c.3414T>G (p.Ser1138Arg)	rs147127279	0.00089
NM_001160372.4(TRAPPC9):c.263C>T (p.Ser88Leu)	rs139631202	0.00069
NM_001160372.4(TRAPPC9):c.1019C>T (p.Ala340Val)	rs143778652	0.00056
NM_001160372.4(TRAPPC9):c.853C>T (p.Arg285Trp)	rs141441030	0.00045
NM_001160372.4(TRAPPC9):c.2077G>A (p.Ala693Thr)	rs147044768	0.00013
NM_001160372.4(TRAPPC9):c.940G>A (p.Ala314Thr)	rs762765901	0.00004

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