List of variants in gene RRM2B reported as likely benign by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_015713.5(RRM2B):c.*190T>C	rs60624814	0.00487
NM_015713.5(RRM2B):c.*1351T>C	rs114108597	0.00478
NM_015713.5(RRM2B):c.2151_2152insA	rs563908556	0.00332
NM_015713.5(RRM2B):c.*1596T>C	rs182874090	0.00086
NM_015713.5(RRM2B):c.*2236A>T	rs566194929	0.00044
NM_015713.5(RRM2B):c.*1867C>T	rs572149875	0.00018
NM_015713.5(RRM2B):c.756G>A (p.Arg252=)	rs377736828	0.00006
NM_015713.5(RRM2B):c.544A>G (p.Thr182Ala)	rs147315735	0.00005
NM_015713.5(RRM2B):c.3003_3004del	rs552260099
NM_015713.5(RRM2B):c.*3489A>G	rs540839717

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