ClinVar Miner

List of variants reported as likely benign for Cornelia de Lange syndrome 2

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_006306.3(SMC1A):c.1098G>A (p.Thr366=) rs140585416
NM_006306.3(SMC1A):c.3663C>T (p.Thr1221=) rs28997583
NM_006306.3(SMC1A):c.63C>T (p.Ile21=) rs781999328

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