List of variants in gene CRADD reported as uncertain significance for carbohydrate metabolism disease

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_003805.5(CRADD):c.497G>A (p.Arg166His)	rs746685035	0.00007
NM_003805.5(CRADD):c.382G>C (p.Gly128Arg)	rs387906861	0.00005
NM_003805.5(CRADD):c.-2A>G	rs1431834925	0.00001
NM_003805.5(CRADD):c.-6-7T>C	rs756888040	0.00001
NM_003805.5(CRADD):c.316A>T (p.Ile106Phe)	rs199846727

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