List of variants in gene RAD21 reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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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.938-11T>C	rs200333487	0.00417
NM_006265.3(RAD21):c.1617A>G (p.Glu539=)	rs138040512	0.00042
NM_006265.3(RAD21):c.735C>T (p.Pro245=)	rs199767556	0.00029
NM_006265.3(RAD21):c.1782C>T (p.Ala594=)	rs61737172	0.00003
NM_006265.3(RAD21):c.93T>C (p.His31=)	rs761516272	0.00002
NM_006265.3(RAD21):c.1162-6del	rs369816312
NM_006265.3(RAD21):c.181_182dup (p.Gly62fs)	rs1554612096
NM_006265.3(RAD21):c.269G>A (p.Arg90Gln)	rs1554612086
NM_006265.3(RAD21):c.56_62del (p.Leu19fs)	rs797045907
NM_006265.3(RAD21):c.579dup (p.Glu194fs)	rs797045908
NM_006265.3(RAD21):c.592_593dup (p.Ser198fs)	rs797045909
NM_006265.3(RAD21):c.785A>T (p.Asp262Val)	rs2130467945

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