List of variants in gene NRXN1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser)	rs200792504	0.00074
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr)	rs199784139	0.00064
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn)	rs80293130	0.00013
NM_001330078.2(NRXN1):c.772+1050C>A	rs367919055	0.00012
NM_001330078.2(NRXN1):c.3532C>A (p.Leu1178Ile)	rs201442938	0.00006
NM_001330078.2(NRXN1):c.348C>A (p.Ser116Arg)	rs764148223	0.00001
NM_001330078.2(NRXN1):c.656_664del (p.Ala219_Glu221del)	rs546508545
NM_001330078.2(NRXN1):c.665_673dup (p.Glu222_Glu224dup)	rs774230140

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