List of variants reported as uncertain significance for autosomal recessive non-syndromic intellectual disability by Centogene AG - the Rare Disease Company

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_017721.5(CC2D1A):c.1357-2A>C	rs200557641	0.00164
NM_017721.5(CC2D1A):c.460G>A (p.Ala154Thr)	rs202025962	0.00007
NM_024989.4(PGAP1):c.843C>A (p.Asp281Glu)	rs1176534322	0.00002
NM_001160372.4(TRAPPC9):c.2551G>A (p.Val851Met)	rs1029565906	0.00001
NM_001160372.4(TRAPPC9):c.2741C>T (p.Thr914Ile)	rs1339133695	0.00001
NM_024989.4(PGAP1):c.1352T>A (p.Phe451Tyr)	rs780043187	0.00001

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