ClinVar Miner

List of variants in gene NLGN4X 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_181332.3(NLGN4X):c.2284C>G (p.Leu762Val)	rs764361221	0.00001
NM_181332.3(NLGN4X):c.1879C>T (p.Arg627Ter)	rs1226379186

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