ClinVar Miner

List of variants in gene CNTN6 reported as likely pathogenic for complex neurodevelopmental disorder

Included ClinVar conditions (295):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NC_000003.12:g.(?_1133359)_(1192637_?)del
NC_000003.12:g.(?_1247669)_(1285156_?)del
NM_001289080.2(CNTN6):c.1492+1G>T

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