ClinVar Miner

List of variants in gene NLGN3 studied for autism, susceptiblity to

Included ClinVar conditions (22):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP gnomAD frequency
NM_181303.2(NLGN3):c.913+11C>G rs202038845 0.00018
NM_181303.2(NLGN3):c.1384G>A (p.Ala462Thr)
NM_181303.2(NLGN3):c.1411C>T (p.Arg471Cys) rs121917893
NM_181303.2(NLGN3):c.163C>T (p.Arg55Ter)
NM_181303.2(NLGN3):c.1672A>G (p.Met558Val) rs2147908798
NM_181303.2(NLGN3):c.2222T>G (p.Leu741Arg)
NM_181303.2(NLGN3):c.611T>C (p.Val204Ala)
NM_181303.2(NLGN3):c.707A>G (p.Asn236Ser) rs2092405042
NM_181303.2(NLGN3):c.806G>A (p.Ser269Asn) rs2092439435
NM_181303.2(NLGN3):c.913+1G>A rs2147900685

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