ClinVar Miner

List of variants in gene NRXN2 reported as likely benign by Genetic Services Laboratory, University of Chicago

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_015080.4(NRXN2):c.531C>T (p.Gly177=) rs2518907 0.58725
NM_015080.4(NRXN2):c.2745C>T (p.Ile915=) rs526338 0.49435
NM_015080.4(NRXN2):c.242T>A (p.Leu81Gln) rs12273892 0.17763
NM_015080.4(NRXN2):c.3327C>T (p.Gly1109=) rs3825074 0.11290
NM_015080.4(NRXN2):c.246G>A (p.Leu82=) rs12293481 0.02638
NM_015080.4(NRXN2):c.3133A>G (p.Ser1045Gly) rs148473653 0.00207
NM_015080.4(NRXN2):c.598G>A (p.Ala200Thr) rs797045803 0.00109
NM_015080.4(NRXN2):c.1090G>A (p.Val364Ile) rs146308270 0.00093
NM_015080.4(NRXN2):c.3651C>T (p.Asn1217=) rs73492149 0.00080
NM_015080.4(NRXN2):c.4847G>T (p.Gly1616Val) rs377164316 0.00029
NM_015080.4(NRXN2):c.999G>A (p.Ser333=) rs375837520 0.00016
NM_015080.4(NRXN2):c.359A>C (p.Asp120Ala) rs1324262269 0.00013
NM_015080.4(NRXN2):c.2883C>T (p.Asn961=) rs184068000 0.00011
NM_015080.4(NRXN2):c.1514C>T (p.Ala505Val) rs200334993 0.00006
NM_015080.4(NRXN2):c.195G>C (p.Leu65=) rs200025059 0.00004
NM_015080.4(NRXN2):c.1851C>T (p.Ser617=) rs546067920 0.00003
NM_015080.4(NRXN2):c.2151C>T (p.Ile717=) rs751918212 0.00001
NM_015080.4(NRXN2):c.3403C>T (p.Pro1135Ser) rs797045800 0.00001
NM_015080.4(NRXN2):c.4035C>T (p.Ser1345=) rs188411090 0.00001

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