ClinVar Miner

List of variants in gene NRXN1 reported as likely pathogenic by Invitae

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Gene type:
ClinVar version:
Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_001330078.2(NRXN1):c.772+1032G>A rs771759988 0.00004
NM_001330078.2(NRXN1):c.772+1133T>C rs1476850082 0.00001
NM_001330078.2(NRXN1):c.832+1G>A rs764621123 0.00001
NC_000002.11:g.(?_50750595)_(50765696_?)del
NC_000002.11:g.(?_50847140)_(50850773_?)dup
NC_000002.11:g.(?_50847140)_(51153113_?)dup
NC_000002.12:g.(?_50236769)_(50346969_?)dup
NM_001330078.2(NRXN1):c.1134+1G>A
NM_001330078.2(NRXN1):c.1135-2A>G rs1679958581
NM_001330078.2(NRXN1):c.1158+23T>G
NM_001330078.2(NRXN1):c.1759+2T>C rs2105344238
NM_001330078.2(NRXN1):c.3070+1G>A
NM_001330078.2(NRXN1):c.3364+1G>A
NM_001330078.2(NRXN1):c.833-2A>C

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