ClinVar Miner

List of variants in gene NRXN1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 145
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HGVS dbSNP
GRCh38/hg38 2p16.3(chr2:49910893-49943628)x3
GRCh38/hg38 2p16.3(chr2:50004126-50041370)x3
GRCh38/hg38 2p16.3(chr2:50265501-50274792)x1
GRCh38/hg38 2p16.3(chr2:50794314-50801971)x1
GRCh38/hg38 2p16.3(chr2:50856272-50882552)x1
NM_001330078.2(NRXN1):c.*13A>C rs199777715
NM_001330078.2(NRXN1):c.*1T>A rs567887770
NM_001330078.2(NRXN1):c.-22C>A rs1057520336
NM_001330078.2(NRXN1):c.-22C>T
NM_001330078.2(NRXN1):c.-7C>A rs202002348
NM_001330078.2(NRXN1):c.-906A>C rs1057522918
NM_001330078.2(NRXN1):c.-919G>C rs1341735881
NM_001330078.2(NRXN1):c.-921-8C>A
NM_001330078.2(NRXN1):c.1050C>G (p.Ala350=) rs201397488
NM_001330078.2(NRXN1):c.108C>T (p.Ala36=) rs199871750
NM_001330078.2(NRXN1):c.1194G>A (p.Thr398=) rs202166616
NM_001330078.2(NRXN1):c.1218C>A (p.Thr406=) rs768225503
NM_001330078.2(NRXN1):c.1227G>A (p.Gly409=) rs779819227
NM_001330078.2(NRXN1):c.1320+10G>A rs113028018
NM_001330078.2(NRXN1):c.1320+19A>G rs201399154
NM_001330078.2(NRXN1):c.1320+4_1320+7dup rs1259067816
NM_001330078.2(NRXN1):c.1320+85C>T
NM_001330078.2(NRXN1):c.1326A>C (p.Val442=) rs201485014
NM_001330078.2(NRXN1):c.1338T>C (p.Asn446=) rs1057523256
NM_001330078.2(NRXN1):c.159G>A (p.Glu53=) rs1057524126
NM_001330078.2(NRXN1):c.1696C>T (p.Leu566=) rs754703742
NM_001330078.2(NRXN1):c.1737C>T (p.Asp579=) rs1202295736
NM_001330078.2(NRXN1):c.1760-11C>G rs199550097
NM_001330078.2(NRXN1):c.1760-15_1760-13del rs1255783166
NM_001330078.2(NRXN1):c.1760-8T>C rs1057522281
NM_001330078.2(NRXN1):c.1779G>A (p.Thr593=) rs200817371
NM_001330078.2(NRXN1):c.1843C>T (p.Leu615=) rs201029409
NM_001330078.2(NRXN1):c.1869T>G (p.Ala623=) rs201816600
NM_001330078.2(NRXN1):c.1887C>T (p.Thr629=) rs200603742
NM_001330078.2(NRXN1):c.1947C>T (p.Ile649=) rs539484479
NM_001330078.2(NRXN1):c.2115A>G (p.Thr705=)
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
NM_001330078.2(NRXN1):c.2143+94A>G
NM_001330078.2(NRXN1):c.2144-22_2144-20del rs779214382
NM_001330078.2(NRXN1):c.2144-4C>A rs1340313788
NM_001330078.2(NRXN1):c.2196C>T (p.Pro732=) rs549242356
NM_001330078.2(NRXN1):c.2244C>G (p.Ser748=) rs761608592
NM_001330078.2(NRXN1):c.2247G>A (p.Gln749=) rs1057521319
NM_001330078.2(NRXN1):c.2301C>A (p.Leu767=) rs1553750260
NM_001330078.2(NRXN1):c.2316C>T (p.Asp772=) rs200449662
NM_001330078.2(NRXN1):c.2348-6A>G rs758131961
NM_001330078.2(NRXN1):c.2375-20C>G rs776794965
NM_001330078.2(NRXN1):c.2375-4A>G rs747910295
NM_001330078.2(NRXN1):c.2391T>A (p.Thr797=) rs750156118
NM_001330078.2(NRXN1):c.2459G>A (p.Ser820Asn) rs80293130
NM_001330078.2(NRXN1):c.2497+187T>G
NM_001330078.2(NRXN1):c.2497+9C>G
NM_001330078.2(NRXN1):c.2498-37G>T
NM_001330078.2(NRXN1):c.249G>T (p.Leu83=) rs565771336
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.261C>T (p.Gly87=) rs587781102
NM_001330078.2(NRXN1):c.273C>T (p.Leu91=) rs201997966
NM_001330078.2(NRXN1):c.285C>T (p.Ile95=) rs759011919
NM_001330078.2(NRXN1):c.2880-22_2880-14del rs755734707
NM_001330078.2(NRXN1):c.2895G>T (p.Val965=) rs199734638
NM_001330078.2(NRXN1):c.297G>A (p.Glu99=) rs1553516705
NM_001330078.2(NRXN1):c.2983A>C (p.Arg995=) rs780193876
NM_001330078.2(NRXN1):c.300T>G (p.Pro100=) rs753793668
NM_001330078.2(NRXN1):c.3030A>G (p.Thr1010=) rs201085950
NM_001330078.2(NRXN1):c.3042C>T (p.Thr1014=) rs75137449
NM_001330078.2(NRXN1):c.3071-10C>T rs398123573
NM_001330078.2(NRXN1):c.3071-17C>G rs200354492
NM_001330078.2(NRXN1):c.3071-58G>A
NM_001330078.2(NRXN1):c.3168T>G (p.Val1056=) rs1553656429
NM_001330078.2(NRXN1):c.3198C>T (p.Ile1066=) rs1553656308
NM_001330078.2(NRXN1):c.3204T>C (p.Asp1068=)
NM_001330078.2(NRXN1):c.3219C>T (p.Asn1073=) rs563089155
NM_001330078.2(NRXN1):c.321G>T (p.Thr107=) rs776382029
NM_001330078.2(NRXN1):c.3228C>A (p.Ile1076=) rs201241923
NM_001330078.2(NRXN1):c.3244+18T>A rs371530345
NM_001330078.2(NRXN1):c.3245-4G>T rs1057520338
NM_001330078.2(NRXN1):c.3330T>C (p.Ser1110=) rs1057522160
NM_001330078.2(NRXN1):c.3365-109705C>G rs1227805288
NM_001330078.2(NRXN1):c.3365-109758A>G rs142041427
NM_001330078.2(NRXN1):c.3365-109836G>A rs747566761
NM_001330078.2(NRXN1):c.3365-109836G>T rs747566761
NM_001330078.2(NRXN1):c.3365-109863C>T rs1057521027
NM_001330078.2(NRXN1):c.3365-109899A>G rs562219421
NM_001330078.2(NRXN1):c.3365-109902_3365-109900dup rs1440459434
NM_001330078.2(NRXN1):c.3365-109992C>T rs796052761
NM_001330078.2(NRXN1):c.3365-110011C>T rs1446478264
NM_001330078.2(NRXN1):c.3365-110014del rs1064794179
NM_001330078.2(NRXN1):c.3365-110016C>T rs1057521771
NM_001330078.2(NRXN1):c.3365-110075G>A
NM_001330078.2(NRXN1):c.3365-110669C>G
NM_001330078.2(NRXN1):c.3365-110728T>A
NM_001330078.2(NRXN1):c.3365-111062G>A
NM_001330078.2(NRXN1):c.3375A>G (p.Thr1125=) rs757748286
NM_001330078.2(NRXN1):c.3384T>C (p.Phe1128=) rs751894635
NM_001330078.2(NRXN1):c.3489C>T (p.Ala1163=) rs147580960
NM_001330078.2(NRXN1):c.3546+115T>A
NM_001330078.2(NRXN1):c.3547-16C>G rs756210249
NM_001330078.2(NRXN1):c.3547-18T>C rs754285936
NM_001330078.2(NRXN1):c.3595G>A (p.Ala1199Thr) rs201336161
NM_001330078.2(NRXN1):c.3654G>C (p.Thr1218=) rs765748728
NM_001330078.2(NRXN1):c.3672C>A (p.Ala1224=) rs201129779
NM_001330078.2(NRXN1):c.3675G>T (p.Thr1225=) rs200179221
NM_001330078.2(NRXN1):c.3717A>T (p.Ala1239=) rs145558855
NM_001330078.2(NRXN1):c.3718+11G>A rs1057522566
NM_001330078.2(NRXN1):c.3808+3dup rs770051379
NM_001330078.2(NRXN1):c.3809-49T>C
NM_001330078.2(NRXN1):c.3888G>A (p.Gln1296=) rs1553535081
NM_001330078.2(NRXN1):c.3936C>T (p.Ala1312=) rs1309946041
NM_001330078.2(NRXN1):c.3957C>T (p.Ala1319=) rs1553534825
NM_001330078.2(NRXN1):c.4107G>A (p.Pro1369=) rs183440866
NM_001330078.2(NRXN1):c.4167C>G (p.Pro1389=) rs143446587
NM_001330078.2(NRXN1):c.4176T>C (p.Asp1392=) rs201135028
NM_001330078.2(NRXN1):c.4428A>G (p.Ala1476=) rs184343684
NM_001330078.2(NRXN1):c.4485C>T (p.Asn1495=) rs200814948
NM_001330078.2(NRXN1):c.537C>T (p.Pro179=) rs771019713
NM_001330078.2(NRXN1):c.576G>A (p.Ser192=)
NM_001330078.2(NRXN1):c.583C>T (p.Leu195=) rs923508164
NM_001330078.2(NRXN1):c.588C>T (p.Pro196=) rs201644834
NM_001330078.2(NRXN1):c.684C>T (p.Cys228=) rs1057520920
NM_001330078.2(NRXN1):c.6G>T (p.Gly2=) rs1015367549
NM_001330078.2(NRXN1):c.702C>T (p.Cys234=) rs200357811
NM_001330078.2(NRXN1):c.723C>G (p.Ala241=) rs200153066
NM_001330078.2(NRXN1):c.726G>A (p.Val242=) rs201349397
NM_001330078.2(NRXN1):c.75G>A (p.Ala25=) rs376641324
NM_001330078.2(NRXN1):c.772+1024C>G rs199645252
NM_001330078.2(NRXN1):c.772+1078A>G rs144049982
NM_001330078.2(NRXN1):c.772+1103T>C rs1553513259
NM_001330078.2(NRXN1):c.772+1118G>A rs201194822
NM_001330078.2(NRXN1):c.772+1392T>C
NM_001330078.2(NRXN1):c.772+16C>T rs1038056478
NM_001330078.2(NRXN1):c.772+6G>C rs777461875
NM_001330078.2(NRXN1):c.772+9C>T rs1297063034
NM_001330078.2(NRXN1):c.773-19C>T rs569755194
NM_001330078.2(NRXN1):c.804G>C (p.Leu268=) rs1553364040
NM_001330078.2(NRXN1):c.821-4A>G
NM_001330078.2(NRXN1):c.832+14T>G rs1057524092
NM_001330078.2(NRXN1):c.832+63A>G
NM_001330078.2(NRXN1):c.833-5T>G rs199712573
NM_001330078.2(NRXN1):c.833-7C>G
NM_001330078.2(NRXN1):c.864A>G (p.Gly288=) rs373654735
NM_001330078.2(NRXN1):c.930G>A (p.Leu310=) rs200532412
NM_001330078.2(NRXN1):c.93G>T (p.Leu31=) rs201539806
NM_001330078.2(NRXN1):c.9G>C (p.Thr3=) rs770820205
NM_138735.4(NRXN1):c.49GCC[12] (p.Gly17[12]) rs750165040
NM_138735.4:(NRXN1):c.49GGC[13] (p.Gly17[13])

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