ClinVar Miner

List of variants in gene NRXN1 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_001135659.2(NRXN1):c.*941dup rs3839057
NM_001330078.2(NRXN1):c.*2511G>C rs148938313
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.3408G>A (p.Thr1136=) rs80094872
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=) rs74714098
NM_001330078.2(NRXN1):c.772+1140G>A rs61658382
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=) rs2303298

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