ClinVar Miner

List of variants in gene NRXN1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 138
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 2p16.3(chr2:50281917-50282100)x3
GRCh37/hg19 2p16.3(chr2:50605728-50618708)x3
GRCh37/hg19 2p16.3(chr2:50816879-50885859)x1
GRCh37/hg19 2p16.3(chr2:50882657-50947044)x1
GRCh37/hg19 2p16.3(chr2:50895613-50947044)x1
GRCh37/hg19 2p16.3(chr2:51070358-51411126)x1
GRCh37/hg19 2p16.3(chr2:51136802-51225497)x3
GRCh37/hg19 2p16.3(chr2:51181831-51520327)x1
GRCh37/hg19 2p16.3(chr2:51191432-51241789)x1
GRCh37/hg19 2p16.3(chr2:51224976-51225497)x0
GRCh37/hg19 2p16.3(chr2:51232182-51326497)x1
GRCh37/hg19 2p16.3(chr2:51241789-51411126)x1
GRCh37/hg19 2p16.3(chr2:51259160-51259694)x3
GRCh38/hg38 2p16.3(chr2:50743524-50780885)x3
GRCh38/hg38 2p16.3(chr2:50822507-50839440)x1
GRCh38/hg38 2p16.3(chr2:50822507-50894953)x1
NM_001330078.2(NRXN1):c.*110G>A rs1045881
NM_001330078.2(NRXN1):c.*1327C>G rs12998798
NM_001330078.2(NRXN1):c.*1365A>G
NM_001330078.2(NRXN1):c.*1539C>G
NM_001330078.2(NRXN1):c.*1692T>C
NM_001330078.2(NRXN1):c.*18G>C rs201303041
NM_001330078.2(NRXN1):c.*1911G>T rs11885824
NM_001330078.2(NRXN1):c.*2105A>C
NM_001330078.2(NRXN1):c.*2372G>A rs116370948
NM_001330078.2(NRXN1):c.*2511G>C rs148938313
NM_001330078.2(NRXN1):c.*2878G>A
NM_001330078.2(NRXN1):c.*540T>A
NM_001330078.2(NRXN1):c.*967_*970dup rs3839058
NM_001330078.2(NRXN1):c.-21C>A rs576405440
NM_001330078.2(NRXN1):c.-281T>C rs35228545
NM_001330078.2(NRXN1):c.-28A>C rs796052760
NM_001330078.2(NRXN1):c.-34C>A rs200335720
NM_001330078.2(NRXN1):c.-421A>C rs67661616
NM_001330078.2(NRXN1):c.-563G>C rs62143025
NM_001330078.2(NRXN1):c.-602G>A rs62143026
NM_001330078.2(NRXN1):c.-883T>C rs10188340
NM_001330078.2(NRXN1):c.-922+7A>C rs200115353
NM_001330078.2(NRXN1):c.-951T>C rs2287235
NM_001330078.2(NRXN1):c.105C>A (p.Gly35=) rs55640811
NM_001330078.2(NRXN1):c.1134+112A>T rs61190471
NM_001330078.2(NRXN1):c.1134+8C>T rs200448187
NM_001330078.2(NRXN1):c.1158+26A>T rs201802152
NM_001330078.2(NRXN1):c.1158+307dup rs67879868
NM_001330078.2(NRXN1):c.1285C>T (p.Pro429Ser) rs78540316
NM_001330078.2(NRXN1):c.1320+147T>C rs72885621
NM_001330078.2(NRXN1):c.1321-212A>G rs13029649
NM_001330078.2(NRXN1):c.1321-229C>T rs13416514
NM_001330078.2(NRXN1):c.1321-56A>C rs13429627
NM_001330078.2(NRXN1):c.1326A>C (p.Val442=) rs201485014
NM_001330078.2(NRXN1):c.1365T>C (p.Leu455=) rs201727684
NM_001330078.2(NRXN1):c.1575A>G (p.Arg525=) rs201941844
NM_001330078.2(NRXN1):c.1760-16C>T rs79422704
NM_001330078.2(NRXN1):c.1760-233A>T rs6545179
NM_001330078.2(NRXN1):c.1833T>C (p.Asp611=) rs190377845
NM_001330078.2(NRXN1):c.1843C>T (p.Leu615=) rs201029409
NM_001330078.2(NRXN1):c.2037G>A (p.Pro679=) rs199714221
NM_001330078.2(NRXN1):c.2109C>T (p.Ser703=) rs200456688
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
NM_001330078.2(NRXN1):c.2143+163T>C rs72882073
NM_001330078.2(NRXN1):c.2143+19A>G rs150513096
NM_001330078.2(NRXN1):c.2193C>T (p.Leu731=) rs201466898
NM_001330078.2(NRXN1):c.222C>T (p.Gly74=) rs201592993
NM_001330078.2(NRXN1):c.2274C>A (p.Thr758=) rs78030925
NM_001330078.2(NRXN1):c.2313A>G (p.Leu771=) rs779330397
NM_001330078.2(NRXN1):c.2347+18C>A rs150460414
NM_001330078.2(NRXN1):c.2375-203A>G rs7571753
NM_001330078.2(NRXN1):c.2385C>G (p.Pro795=) rs147984237
NM_001330078.2(NRXN1):c.2421C>T (p.Asn807=) rs115211871
NM_001330078.2(NRXN1):c.2497+88C>A rs13008919
NM_001330078.2(NRXN1):c.2498-300G>C rs13001103
NM_001330078.2(NRXN1):c.2498-302G>T rs13001104
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met) rs201818223
NM_001330078.2(NRXN1):c.261C>A (p.Gly87=) rs587781102
NM_001330078.2(NRXN1):c.2730G>A (p.Lys910=) rs192909520
NM_001330078.2(NRXN1):c.2772C>T (p.Tyr924=) rs200182626
NM_001330078.2(NRXN1):c.2879+182T>C rs13386253
NM_001330078.2(NRXN1):c.2879+20A>G rs200986624
NM_001330078.2(NRXN1):c.2879+231T>C rs13386159
NM_001330078.2(NRXN1):c.3045C>T (p.Ala1015=) rs56402642
NM_001330078.2(NRXN1):c.3070+115C>A rs2241175
NM_001330078.2(NRXN1):c.3071-149G>A rs2075233
NM_001330078.2(NRXN1):c.3071-281A>G rs6704933
NM_001330078.2(NRXN1):c.3071-284G>A rs2075232
NM_001330078.2(NRXN1):c.3090A>C (p.Gly1030=) rs201886024
NM_001330078.2(NRXN1):c.3129A>G (p.Val1043=) rs200698497
NM_001330078.2(NRXN1):c.3201C>T (p.Ser1067=) rs75275592
NM_001330078.2(NRXN1):c.3219C>T (p.Asn1073=) rs563089155
NM_001330078.2(NRXN1):c.3244+129C>A rs59507529
NM_001330078.2(NRXN1):c.3244+131A>T rs2075234
NM_001330078.2(NRXN1):c.3244+231G>T rs59300829
NM_001330078.2(NRXN1):c.3245-241T>C rs13398860
NM_001330078.2(NRXN1):c.3249C>T (p.Pro1083=) rs116236999
NM_001330078.2(NRXN1):c.324G>A (p.Pro108=) rs199595253
NM_001330078.2(NRXN1):c.3364+121A>T rs12713101
NM_001330078.2(NRXN1):c.3364+20T>C rs3213756
NM_001330078.2(NRXN1):c.3365-109703A>T rs199700602
NM_001330078.2(NRXN1):c.3365-109709A>G rs13023114
NM_001330078.2(NRXN1):c.3365-109830G>A rs148517834
NM_001330078.2(NRXN1):c.3365-109893G>A rs546558752
NM_001330078.2(NRXN1):c.3365-109930G>T rs13413205
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=) rs80094872
NM_001330078.2(NRXN1):c.3546+226T>C rs1618655
NM_001330078.2(NRXN1):c.3546+227C>T rs11889906
NM_001330078.2(NRXN1):c.3547-162G>A rs78497262
NM_001330078.2(NRXN1):c.3547-29C>G rs74387895
NM_001330078.2(NRXN1):c.3547-313T>C rs73932925
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=) rs79970751
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=) rs74714098
NM_001330078.2(NRXN1):c.4216+113C>G rs1345562
NM_001330078.2(NRXN1):c.4216+17T>A rs200836763
NM_001330078.2(NRXN1):c.4217-121T>C rs17039448
NM_001330078.2(NRXN1):c.4217-13C>T rs376269786
NM_001330078.2(NRXN1):c.4217-16A>C rs74520052
NM_001330078.2(NRXN1):c.4236C>T (p.Gly1412=) rs587781101
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=) rs55923848
NM_001330078.2(NRXN1):c.4275G>T (p.Arg1425=) rs143495349
NM_001330078.2(NRXN1):c.4338T>C (p.Leu1446=) rs796052759
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=) rs112536447
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=) rs113380721
NM_001330078.2(NRXN1):c.498G>A (p.Ala166=) rs201212909
NM_001330078.2(NRXN1):c.501C>G (p.Leu167=) rs200248561
NM_001330078.2(NRXN1):c.511C>T (p.Leu171=) rs1045874
NM_001330078.2(NRXN1):c.600C>T (p.Gly200=) rs201481698
NM_001330078.2(NRXN1):c.772+1015C>A rs200375396
NM_001330078.2(NRXN1):c.772+102G>C rs13426386
NM_001330078.2(NRXN1):c.772+1140G>A rs61658382
NM_001330078.2(NRXN1):c.772+1407C>G rs79697415
NM_001330078.2(NRXN1):c.772+162C>T rs13023341
NM_001330078.2(NRXN1):c.798G>A (p.Ala266=) rs201027928
NM_001330078.2(NRXN1):c.821-54A>G rs7423296
NM_001330078.2(NRXN1):c.821-84A>G rs4327263
NM_001330078.2(NRXN1):c.832+135A>T rs36106628
NM_001330078.2(NRXN1):c.832+267C>T rs62142981
NM_001330078.2(NRXN1):c.882C>T (p.Tyr294=) rs200464704
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298
NM_138735.4(NRXN1):c.49GGC[7] (p.Gly17[7]) rs750165040
NM_138735.4(NRXN1):c.49[5] (p.Gly17[5]) rs750165040

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.