ClinVar Miner

List of variants in gene NRXN1 reported as uncertain significance by GeneDx

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Total variants: 107
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HGVS dbSNP
NM_001135659.2(NRXN1):c.1322C>T (p.Thr441Met) rs796052764
NM_001135659.2(NRXN1):c.1364A>G (p.Tyr455Cys) rs371321580
NM_001135659.2(NRXN1):c.1412G>A (p.Ser471Asn) rs796052788
NM_001135659.2(NRXN1):c.1427G>A (p.Gly476Asp) rs1057520337
NM_001135659.2(NRXN1):c.1502C>T (p.Pro501Leu) rs530674644
NM_001135659.2(NRXN1):c.150C>G (p.Cys50Trp) rs1057518563
NM_001135659.2(NRXN1):c.1547T>G (p.Val516Gly) rs1553778755
NM_001135659.2(NRXN1):c.1564A>T (p.Ile522Phe) rs796052767
NM_001135659.2(NRXN1):c.1600C>T (p.Pro534Ser) rs199834999
NM_001135659.2(NRXN1):c.1686C>T (p.Gly562=) rs199701804
NM_001135659.2(NRXN1):c.1709C>A (p.Ala570Asp) rs529697285
NM_001135659.2(NRXN1):c.1712A>G (p.Lys571Arg) rs796052769
NM_001135659.2(NRXN1):c.1898C>T (p.Thr633Met) rs201530175
NM_001135659.2(NRXN1):c.1904G>A (p.Arg635His) rs761279630
NM_001135659.2(NRXN1):c.1918G>T (p.Ala640Ser) rs796052770
NM_001135659.2(NRXN1):c.1942G>A (p.Asp648Asn) rs796052771
NM_001135659.2(NRXN1):c.1970G>C (p.Gly657Ala) rs780931684
NM_001135659.2(NRXN1):c.208T>C (p.Phe70Leu) rs796052773
NM_001135659.2(NRXN1):c.219G>C (p.Glu73Asp) rs201031680
NM_001135659.2(NRXN1):c.2230G>A (p.Gly744Arg) rs757547387
NM_001135659.2(NRXN1):c.2240A>C (p.Tyr747Ser) rs752073539
NM_001135659.2(NRXN1):c.2330C>T (p.Thr777Met) rs199970666
NM_001135659.2(NRXN1):c.2348C>A (p.Ser783Tyr) rs796052774
NM_001135659.2(NRXN1):c.23G>T (p.Arg8Leu) rs796052765
NM_001135659.2(NRXN1):c.2437G>A (p.Ala813Thr) rs199548487
NM_001135659.2(NRXN1):c.2495-10T>A rs1085307863
NM_001135659.2(NRXN1):c.2495-7T>A rs199673405
NM_001135659.2(NRXN1):c.2542G>A (p.Glu848Lys) rs202145311
NM_001135659.2(NRXN1):c.2617+3A>G rs202074070
NM_001135659.2(NRXN1):c.2627C>T (p.Ala876Val) rs199557987
NM_001135659.2(NRXN1):c.262C>G (p.Arg88Gly) rs748684256
NM_001135659.2(NRXN1):c.2652C>G (p.Phe884Leu) rs796052789
NM_001135659.2(NRXN1):c.2686C>T (p.Arg896Trp) rs796052777
NM_001135659.2(NRXN1):c.2690A>G (p.Tyr897Cys) rs796052778
NM_001135659.2(NRXN1):c.2717T>C (p.Ile906Thr) rs796052779
NM_001135659.2(NRXN1):c.2779G>A (p.Asp927Asn) rs796052780
NM_001135659.2(NRXN1):c.28G>A (p.Gly10Ser) rs777530225
NM_001135659.2(NRXN1):c.2902C>T (p.His968Tyr) rs1057524516
NM_001135659.2(NRXN1):c.2905C>A (p.Leu969Ile) rs794727140
NM_001135659.2(NRXN1):c.2935G>A (p.Asp979Asn) rs796052781
NM_001135659.2(NRXN1):c.2963A>G (p.Asp988Gly) rs1057518283
NM_001135659.2(NRXN1):c.3013G>T (p.Val1005Leu) rs1057524337
NM_001135659.2(NRXN1):c.3099A>G (p.Ile1033Met) rs796052782
NM_001135659.2(NRXN1):c.3150_3161dup (p.Thr1051_Thr1054dup) rs1553698269
NM_001135659.2(NRXN1):c.3152C>T (p.Thr1051Met) rs199980022
NM_001135659.2(NRXN1):c.3223A>G (p.Thr1075Ala) rs753262049
NM_001135659.2(NRXN1):c.322C>G (p.Pro108Ala) rs199784029
NM_001135659.2(NRXN1):c.325G>A (p.Val109Ile) rs779979011
NM_001135659.2(NRXN1):c.32G>A (p.Cys11Tyr) rs796052766
NM_001135659.2(NRXN1):c.3374C>T (p.Thr1125Ile) rs796052784
NM_001135659.2(NRXN1):c.3401A>G (p.Asn1134Ser) rs201963074
NM_001135659.2(NRXN1):c.3485-109897G>C rs777054372
NM_001135659.2(NRXN1):c.3485-109897G>T rs777054372
NM_001135659.2(NRXN1):c.3485-109912G>A rs1057524649
NM_001135659.2(NRXN1):c.3485-109922G>C rs1188018101
NM_001135659.2(NRXN1):c.3485-109939C>T rs766942777
NM_001135659.2(NRXN1):c.3485-109977G>A rs1057517946
NM_001135659.2(NRXN1):c.353G>A (p.Arg118His) rs796052775
NM_001135659.2(NRXN1):c.3599A>G (p.Gln1200Arg) rs768319291
NM_001135659.2(NRXN1):c.3662A>G (p.His1221Arg) rs200915287
NM_001135659.2(NRXN1):c.369C>A (p.Phe123Leu) rs879210752
NM_001135659.2(NRXN1):c.3736A>G (p.Ile1246Val) rs751778015
NM_001135659.2(NRXN1):c.374A>G (p.Asn125Ser) rs770641207
NM_001135659.2(NRXN1):c.3773C>T (p.Thr1258Met) rs201720955
NM_001135659.2(NRXN1):c.407A>G (p.Lys136Arg) rs202118977
NM_001135659.2(NRXN1):c.4124C>T (p.Thr1375Ile) rs200672080
NM_001135659.2(NRXN1):c.4131G>C (p.Glu1377Asp) rs200935246
NM_001135659.2(NRXN1):c.4132T>G (p.Ser1378Ala) rs1064796707
NM_001135659.2(NRXN1):c.4149G>A (p.Met1383Ile) rs146100580
NM_001135659.2(NRXN1):c.4322G>A (p.Ser1441Asn) rs796052762
NM_001135659.2(NRXN1):c.4357G>A (p.Gly1453Ser) rs200604893
NM_001135659.2(NRXN1):c.4394G>A (p.Arg1465Gln) rs201559515
NM_001135659.2(NRXN1):c.4614_4616del (p.Lys1539del) rs796052785
NM_001135659.2(NRXN1):c.476C>T (p.Pro159Leu) rs373070672
NM_001135659.2(NRXN1):c.503A>G (p.Lys168Arg) rs200625614
NM_001135659.2(NRXN1):c.570C>A (p.Asn190Lys) rs564945882
NM_001135659.2(NRXN1):c.587C>T (p.Pro196Leu) rs199836119
NM_001135659.2(NRXN1):c.637G>A (p.Gly213Arg) rs199561088
NM_001135659.2(NRXN1):c.656_664del (p.Ala219_Glu221del) rs546508545
NM_001135659.2(NRXN1):c.76G>C (p.Glu26Gln) rs201847846
NM_001135659.2(NRXN1):c.772G>A (p.Glu258Lys) rs746465882
NM_001135659.2(NRXN1):c.780A>T (p.Lys260Asn) rs201741449
NM_001135659.2(NRXN1):c.821A>G (p.Asn274Ser) rs759434607
NM_001135659.2(NRXN1):c.878A>C (p.Asn293Thr) rs779434583
NM_001135659.2(NRXN1):c.880A>G (p.Asn294Asp) rs781179797
NM_001135659.2(NRXN1):c.904A>T (p.Met302Leu) rs776779952
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152
NM_001330078.2(NRXN1):c.1400_1401inv (p.Gly467Val) rs796052786
NM_001330078.2(NRXN1):c.1541A>G (p.Asn514Ser) rs770389634
NM_001330078.2(NRXN1):c.1688T>C (p.Ile563Thr) rs201837579
NM_001330078.2(NRXN1):c.1945A>G (p.Ile649Val) rs200074974
NM_001330078.2(NRXN1):c.1978G>A (p.Ala660Thr) rs199939303
NM_001330078.2(NRXN1):c.2036C>T (p.Pro679Leu) rs201735573
NM_001330078.2(NRXN1):c.2190G>T (p.Gln730His) rs199978276
NM_001330078.2(NRXN1):c.2414A>G (p.Asn805Ser) rs753087756
NM_001330078.2(NRXN1):c.2533C>T (p.His845Tyr) rs199784139
NM_001330078.2(NRXN1):c.270G>T (p.Gln90His) rs199960045
NM_001330078.2(NRXN1):c.302C>G (p.Ala101Gly) rs200184823
NM_001330078.2(NRXN1):c.3202G>A (p.Asp1068Asn) rs200722697
NM_001330078.2(NRXN1):c.322C>T (p.Pro108Ser) rs199784029
NM_001330078.2(NRXN1):c.3905A>G (p.Tyr1302Cys) rs761776814
NM_001330078.2(NRXN1):c.569A>G (p.Asn190Ser) rs200792504
NM_001330078.2(NRXN1):c.600C>T (p.Gly200=) rs201481698
NM_001330078.2(NRXN1):c.739C>G (p.Arg247Gly) rs200009780
NM_001330078.2(NRXN1):c.749T>A (p.Phe250Tyr) rs200646155
NM_001330078.2(NRXN1):c.752G>A (p.Arg251His) rs780954241
NM_001330078.2(NRXN1):c.772+1050C>A rs367919055

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