ClinVar Miner

List of variants in gene combination LOC126861232, NRXN2 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015080.4(NRXN2):c.2281A>T (p.Met761Leu)	rs138291758	0.00014
NM_015080.4(NRXN2):c.2193G>A (p.Thr731=)	rs201783047	0.00001
NM_015080.4(NRXN2):c.2226G>A (p.Lys742=)	rs768605786	0.00001

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