ClinVar Miner

List of variants in gene NLGN3 studied for neurodevelopmental disorder

Included ClinVar conditions (779):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_181303.2(NLGN3):c.1373A>T (p.Tyr458Phe)
NM_181303.2(NLGN3):c.1978C>T (p.Arg660Cys)
NM_181303.2(NLGN3):c.2161C>T (p.Leu721Phe) rs2092463681
NM_181303.2(NLGN3):c.2389C>T (p.Arg797Trp)
NM_181303.2(NLGN3):c.814A>T (p.Ile272Phe) rs2147900298

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