ClinVar Miner

List of variants reported as likely pathogenic for Autism, susceptibility to, X-linked 1

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_181303.2(NLGN3):c.1672A>G (p.Met558Val)	rs2147908798
NM_181303.2(NLGN3):c.2222T>G (p.Leu741Arg)	rs1460006418
NM_181303.2(NLGN3):c.913+1G>A	rs2147900685

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