ClinVar Miner

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

Included ClinVar conditions (1350):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_006265.3(RAD21):c.-32-1G>A rs16889042 0.00127
NM_006265.3(RAD21):c.1705-12G>A rs189362023 0.00034
NM_006265.3(RAD21):c.735C>T (p.Pro245=) rs199767556 0.00029
NM_006265.3(RAD21):c.1185G>A (p.Pro395=) rs138247094 0.00026
NM_006265.3(RAD21):c.1503T>G (p.Pro501=) rs150935041 0.00017
NM_006265.3(RAD21):c.159A>G (p.Leu53=) rs186566723 0.00011
NM_006265.3(RAD21):c.645T>C (p.Tyr215=) rs143910582 0.00010
NM_006265.3(RAD21):c.450G>A (p.Gly150=) rs188711205 0.00009
NM_006265.3(RAD21):c.1471-16T>C rs202211817 0.00008
NM_006265.3(RAD21):c.540C>T (p.Asp180=) rs761693720 0.00006
NM_006265.3(RAD21):c.1221A>G (p.Gly407=) rs147090806 0.00004
NM_006265.3(RAD21):c.1471-3A>G rs202098276 0.00004
NM_006265.3(RAD21):c.393G>A (p.Gln131=) rs759582860 0.00004
NM_006265.3(RAD21):c.807T>C (p.Asn269=) rs372221161 0.00004
NM_006265.3(RAD21):c.999T>C (p.Asp333=) rs768725843 0.00004
NM_006265.3(RAD21):c.1782C>T (p.Ala594=) rs61737172 0.00003
NM_006265.3(RAD21):c.363G>C (p.Leu121=) rs959964243 0.00003
NM_006265.3(RAD21):c.741C>G (p.Ala247=) rs141798668 0.00003
NM_006265.3(RAD21):c.849C>T (p.Pro283=) rs369661655 0.00003
NM_006265.3(RAD21):c.1471-9T>C rs763912364 0.00002
NM_006265.3(RAD21):c.1629T>C (p.Asp543=) rs377080076 0.00002
NM_006265.3(RAD21):c.717C>T (p.Gly239=) rs1293278125 0.00002
NM_006265.3(RAD21):c.1065G>A (p.Pro355=) rs202233096 0.00001
NM_006265.3(RAD21):c.1068C>T (p.Pro356=) rs1348606480 0.00001
NM_006265.3(RAD21):c.1349G>A (p.Arg450His) rs1051321465 0.00001
NM_006265.3(RAD21):c.1848G>A (p.Pro616=) rs761965871 0.00001
NM_006265.3(RAD21):c.1162-20_1162-18del
NM_006265.3(RAD21):c.12A>C (p.Ala4=)
NM_006265.3(RAD21):c.1317T>C (p.Val439=)
NM_006265.3(RAD21):c.1322-14A>G
NM_006265.3(RAD21):c.1322-5T>G
NM_006265.3(RAD21):c.1322-6T>C
NM_006265.3(RAD21):c.1329C>G (p.Pro443=) rs765533095
NM_006265.3(RAD21):c.1353C>T (p.Leu451=)
NM_006265.3(RAD21):c.1425A>T (p.Gly475=)
NM_006265.3(RAD21):c.1470+13A>G
NM_006265.3(RAD21):c.1470+20C>T
NM_006265.3(RAD21):c.1471-13G>A
NM_006265.3(RAD21):c.1500A>G (p.Pro500=)
NM_006265.3(RAD21):c.1560_1583dup (p.Glu528_Lys529insLeuLeuProGluLysGluLysGlu)
NM_006265.3(RAD21):c.165A>G (p.Thr55=)
NM_006265.3(RAD21):c.1705-15T>C
NM_006265.3(RAD21):c.1719A>G (p.Lys573=)
NM_006265.3(RAD21):c.1824T>G (p.Ala608=)
NM_006265.3(RAD21):c.1845A>G (p.Glu615=)
NM_006265.3(RAD21):c.1863C>T (p.Ile621=)
NM_006265.3(RAD21):c.228A>T (p.Ala76=) rs2130479411
NM_006265.3(RAD21):c.351T>C (p.Phe117=)
NM_006265.3(RAD21):c.374+13T>C
NM_006265.3(RAD21):c.375-12C>T
NM_006265.3(RAD21):c.375-9_375-7del
NM_006265.3(RAD21):c.42G>C (p.Leu14=)
NM_006265.3(RAD21):c.481+8A>C
NM_006265.3(RAD21):c.482-15_482-11del rs750504354
NM_006265.3(RAD21):c.482-19C>T
NM_006265.3(RAD21):c.482-3del rs1217367738
NM_006265.3(RAD21):c.564T>G (p.Thr188=)
NM_006265.3(RAD21):c.576A>G (p.Leu192=)
NM_006265.3(RAD21):c.689-15C>T
NM_006265.3(RAD21):c.689-16dup rs773593714
NM_006265.3(RAD21):c.689-17del
NM_006265.3(RAD21):c.689-4del
NM_006265.3(RAD21):c.699T>C (p.Leu233=)
NM_006265.3(RAD21):c.714T>C (p.Asp238=)
NM_006265.3(RAD21):c.741C>A (p.Ala247=)
NM_006265.3(RAD21):c.744C>T (p.Leu248=)
NM_006265.3(RAD21):c.815-17_815-5del rs35902828
NM_006265.3(RAD21):c.815-27dup rs35902828
NM_006265.3(RAD21):c.815-5del rs35902828
NM_006265.3(RAD21):c.815-6T>A
NM_006265.3(RAD21):c.815-6_815-5del rs35902828
NM_006265.3(RAD21):c.81A>C (p.Leu27=)
NM_006265.3(RAD21):c.937+10T>C
NM_006265.3(RAD21):c.937+7A>G
NM_006265.3(RAD21):c.948A>G (p.Thr316=)
NM_006265.3(RAD21):c.9C>T (p.Tyr3=)

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