ClinVar Miner

List of variants in gene NRXN1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP
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
NM_001330078.2(NRXN1):c.-281T>C rs35228545
NM_001330078.2(NRXN1):c.-602G>A rs62143026
NM_001330078.2(NRXN1):c.-883T>C rs10188340
NM_001330078.2(NRXN1):c.1134+112A>T
NM_001330078.2(NRXN1):c.1158+307dup
NM_001330078.2(NRXN1):c.1320+147T>C
NM_001330078.2(NRXN1):c.1321-212A>G
NM_001330078.2(NRXN1):c.1321-229C>T
NM_001330078.2(NRXN1):c.1321-56A>C
NM_001330078.2(NRXN1):c.1760-233A>T
NM_001330078.2(NRXN1):c.2122C>A (p.Leu708Ile) rs56086732
NM_001330078.2(NRXN1):c.2143+163T>C
NM_001330078.2(NRXN1):c.2375-203A>G
NM_001330078.2(NRXN1):c.2497+88C>A
NM_001330078.2(NRXN1):c.2498-300G>C
NM_001330078.2(NRXN1):c.2498-302G>T
NM_001330078.2(NRXN1):c.2879+182T>C
NM_001330078.2(NRXN1):c.2879+231T>C
NM_001330078.2(NRXN1):c.3070+115C>A
NM_001330078.2(NRXN1):c.3071-149G>A
NM_001330078.2(NRXN1):c.3071-281A>G
NM_001330078.2(NRXN1):c.3071-284G>A
NM_001330078.2(NRXN1):c.3244+129C>A
NM_001330078.2(NRXN1):c.3244+131A>T
NM_001330078.2(NRXN1):c.3244+231G>T
NM_001330078.2(NRXN1):c.3245-241T>C
NM_001330078.2(NRXN1):c.3364+121A>T
NM_001330078.2(NRXN1):c.3546+226T>C
NM_001330078.2(NRXN1):c.3546+227C>T
NM_001330078.2(NRXN1):c.3547-162G>A
NM_001330078.2(NRXN1):c.3547-29C>G
NM_001330078.2(NRXN1):c.3547-313T>C
NM_001330078.2(NRXN1):c.4216+113C>G
NM_001330078.2(NRXN1):c.4217-121T>C
NM_001330078.2(NRXN1):c.772+102G>C
NM_001330078.2(NRXN1):c.772+1407C>G
NM_001330078.2(NRXN1):c.772+162C>T
NM_001330078.2(NRXN1):c.821-54A>G
NM_001330078.2(NRXN1):c.821-84A>G
NM_001330078.2(NRXN1):c.832+135A>T
NM_001330078.2(NRXN1):c.832+267C>T

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