List of variants in gene RAD21 reported as likely pathogenic for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006265.3(RAD21):c.1306C>T (p.Gln436Ter)	rs1563688680
NM_006265.3(RAD21):c.1432C>T (p.Arg478Ter)	rs748575266
NM_006265.3(RAD21):c.1753T>C (p.Cys585Arg)	rs387907213
NM_006265.3(RAD21):c.428T>C (p.Ile143Thr)	rs1382274750

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