List of variants in gene RELB reported as benign for not provided

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_006509.4(RELB):c.1347C>T (p.His449=)	rs2230682	0.00909
NM_006509.4(RELB):c.405G>A (p.Gln135=)	rs148422079	0.00365
NM_006509.4(RELB):c.357G>A (p.Pro119=)	rs35336204	0.00234
NM_006509.4(RELB):c.1491A>G (p.Thr497=)	rs200818596	0.00163
NM_006509.4(RELB):c.1563C>T (p.Ala521=)	rs199742203	0.00161
NM_006509.4(RELB):c.1264C>T (p.Leu422=)	rs34942687	0.00055
NM_006509.4(RELB):c.219G>T (p.Pro73=)	rs765088332	0.00032
NM_006509.4(RELB):c.108G>A (p.Gly36=)	rs191212936	0.00009
NM_006509.4(RELB):c.975C>T (p.Cys325=)	rs61759894	0.00003
NM_006509.4(RELB):c.1458C>T (p.Asp486=)	rs77076601
NM_006509.4(RELB):c.504+21del
NM_006509.4(RELB):c.663-14C>T	rs34954034

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