ClinVar Miner

List of variants in gene NRXN1 reported as pathogenic for brain disorder

Included ClinVar conditions (1834):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NC_000002.12:g.(?_50721552)_(50944617_?)del
NM_001135659.3:c.(?_-921)_(931+1_932-1)del
NM_001330078.2(NRXN1):c.1066del (p.Glu356fs)
NM_001330078.2(NRXN1):c.3430C>T (p.Arg1144Ter) rs1282230077
NM_001330078.2(NRXN1):c.471dup (p.Leu158fs)
NM_001330078.2(NRXN1):c.773-1G>T rs1574949440
Single allele

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