ClinVar Miner

Submissions for variant NM_000435.3(NOTCH3):c.1162T>C (p.Cys388Arg)

dbSNP: rs1599391938
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV001003545 SCV001161889 likely pathogenic Migraine with aura; Abnormal cerebral white matter morphology no assertion criteria provided research

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