List of variants in gene RRM2B reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_015713.5(RRM2B):c.846G>C (p.Met282Ile)	rs182614164	0.00005
NM_015713.5(RRM2B):c.790-2A>G	rs1441534206
NM_015713.5(RRM2B):c.875_876del (p.Arg292fs)

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