ClinVar Miner

List of variants studied for Intellectual disability, autosomal recessive 13 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_001160372.4(TRAPPC9):c.2892G>T (p.Lys964Asn) rs780699195 0.00001
NM_001160372.4(TRAPPC9):c.1099T>G (p.Phe367Val) rs2540230814
NM_001160372.4(TRAPPC9):c.3292G>C (p.Gly1098Arg) rs536787964

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