ClinVar Miner

List of variants in gene RAD21 reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_006265.3(RAD21):c.1440T>C (p.Ala480=) rs1050838 0.13137
NM_006265.3(RAD21):c.688+8G>A rs2921787 0.11506
NM_006265.3(RAD21):c.1242T>G (p.Asp414Glu) rs75160167 0.00623
NM_006265.3(RAD21):c.938-11T>C rs200333487 0.00417
NM_006265.3(RAD21):c.786C>T (p.Asp262=) rs34653007 0.00300
NM_006265.3(RAD21):c.1515C>G (p.Pro505=) rs9297560 0.00298
NM_006265.3(RAD21):c.1471-11A>G rs112473657 0.00068
NM_006265.3(RAD21):c.468A>G (p.Gln156=) rs530697556 0.00045
NM_006265.3(RAD21):c.1617A>G (p.Glu539=) rs138040512 0.00042
NM_006265.3(RAD21):c.582G>A (p.Glu194=) rs201468757 0.00008
NM_006265.3(RAD21):c.1237T>C (p.Leu413=) rs201779352 0.00003
NM_006265.3(RAD21):c.145-4A>G rs752213732 0.00002
NM_006265.3(RAD21):c.1564C>G (p.Leu522Val)
NM_006265.3(RAD21):c.1620+11_1620+14del
NM_006265.3(RAD21):c.274+26GTT[5] rs112562183
NM_006265.3(RAD21):c.689-15C>A
NM_006265.3(RAD21):c.815-10_815-5del rs35902828
NM_006265.3(RAD21):c.815-15_815-5del
NM_006265.3(RAD21):c.815-5del rs35902828
NM_006265.3(RAD21):c.815-6_815-5del rs35902828
NM_006265.3(RAD21):c.938-14del

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