List of variants in gene combination RBPJL, SDC4 reported as benign by Diabetes Molecular Genetics Section, Phoenix Epidemiology and Clinical Research Branch, National Institutes of Health

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_002999.4(SDC4):c.445+251C>T	rs2425696	0.75835
NM_002999.4(SDC4):c.199+134A>G	rs2072792	0.48742
NM_002999.4(SDC4):c.446-1455C>T	rs985586	0.26964
NM_002999.4(SDC4):c.61-965T>C	rs147593522	0.00361
NM_002999.4(SDC4):c.61-4447del	rs148973596

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