List of variants in gene RAD51B reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_133510.4(RAD51B):c.1036+3907G>A	rs117190791	0.01690
NM_133510.4(RAD51B):c.756+112979T>C	rs117405447	0.00368
NM_133510.4(RAD51B):c.854-24328T>C	rs184721768	0.00100
NM_133510.4(RAD51B):c.85-62T>C	rs574178911	0.00083
NM_133510.4(RAD51B):c.757-92T>C	rs533348490	0.00051
NM_133510.4(RAD51B):c.854-24150C>A	rs556371643	0.00007
NM_133510.4(RAD51B):c.452+3A>G	rs753393344	0.00005
NM_133510.4(RAD51B):c.958-29A>T	rs34436700

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