ClinVar Miner

List of variants in gene RAD21 reported as uncertain significance for Cornelia de Lange syndrome

Included ClinVar conditions (10):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_006265.2(RAD21):c.1349G>A (p.Arg450His) rs1051321465
NM_006265.2(RAD21):c.1352T>G (p.Leu451Arg) rs144953114
NM_006265.2(RAD21):c.145-4A>G rs752213732
NM_006265.2(RAD21):c.1576G>C (p.Glu526Gln) rs373026310
NM_006265.2(RAD21):c.1617A>G (p.Glu539=) rs138040512
NM_006265.2(RAD21):c.1782C>T (p.Ala594=) rs61737172
NM_006265.2(RAD21):c.1852A>G (p.Ser618Gly) rs1554610467

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