ClinVar Miner

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

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 50
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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.3213C>G (p.Leu1071=) rs139264192 0.00202
NM_015080.4(NRXN2):c.598G>A (p.Ala200Thr) rs797045803 0.00109
NM_015080.4(NRXN2):c.2918+6G>A rs144906809 0.00103
NM_015080.4(NRXN2):c.1090G>A (p.Val364Ile) rs146308270 0.00093
NM_015080.4(NRXN2):c.3757+9C>T rs376552947 0.00086
NM_015080.4(NRXN2):c.3651C>T (p.Asn1217=) rs73492149 0.00080
NM_015080.4(NRXN2):c.2441C>T (p.Ala814Val) rs200231532 0.00041
NM_015080.4(NRXN2):c.4847G>T (p.Gly1616Val) rs377164316 0.00029
NM_015080.4(NRXN2):c.376C>A (p.Leu126Met) rs370521049 0.00026
NM_015080.4(NRXN2):c.894C>T (p.Phe298=) rs137891559 0.00020
NM_015080.4(NRXN2):c.999G>A (p.Ser333=) rs375837520 0.00016
NM_015080.4(NRXN2):c.49C>G (p.Leu17Val) rs797045802 0.00015
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.1564C>T (p.Arg522Cys) rs201258323 0.00006
NM_015080.4(NRXN2):c.2463T>C (p.Asn821=) rs71579857 0.00006
NM_015080.4(NRXN2):c.3228A>G (p.Pro1076=) rs371180957 0.00006
NM_015080.4(NRXN2):c.2044G>A (p.Val682Ile) rs1056113277 0.00005
NM_015080.4(NRXN2):c.1522C>T (p.Arg508Cys) rs200169230 0.00004
NM_015080.4(NRXN2):c.195G>C (p.Leu65=) rs200025059 0.00004
NM_015080.4(NRXN2):c.3368C>T (p.Thr1123Ile) rs187397245 0.00004
NM_015080.4(NRXN2):c.1838C>T (p.Ala613Val) rs748162664 0.00003
NM_015080.4(NRXN2):c.1851C>T (p.Ser617=) rs546067920 0.00003
NM_015080.4(NRXN2):c.2677A>G (p.Met893Val) rs765465352 0.00003
NM_015080.4(NRXN2):c.4437C>T (p.Ala1479=) rs71579869 0.00003
NM_015080.4(NRXN2):c.670C>T (p.Pro224Ser) rs772811573 0.00003
NM_015080.4(NRXN2):c.3965C>T (p.Ala1322Val) rs375639642 0.00002
NM_015080.4(NRXN2):c.1286T>C (p.Ile429Thr) rs797045798 0.00001
NM_015080.4(NRXN2):c.1580A>G (p.Asn527Ser) rs181686738 0.00001
NM_015080.4(NRXN2):c.1963G>A (p.Val655Met) rs764854618 0.00001
NM_015080.4(NRXN2):c.2124C>T (p.Gly708=) rs146517173 0.00001
NM_015080.4(NRXN2):c.2151C>T (p.Ile717=) rs751918212 0.00001
NM_015080.4(NRXN2):c.234G>A (p.Leu78=) rs748442370 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
NM_015080.4(NRXN2):c.1139G>A (p.Arg380Gln) rs587780408
NM_015080.4(NRXN2):c.2537-8C>T rs797045799
NM_015080.4(NRXN2):c.3851G>T (p.Arg1284Leu) rs587780409
NM_015080.4(NRXN2):c.4046G>A (p.Ser1349Asn) rs552728515
NM_015080.4(NRXN2):c.4519C>T (p.Pro1507Ser) rs749398433
NM_015080.4(NRXN2):c.4622A>T (p.Asp1541Val) rs797045801
NM_015080.4(NRXN2):c.749G>C (p.Gly250Ala) rs2135588749
NM_015080.4(NRXN2):c.851-8G>A rs371081453

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