List of variants in gene SDK2 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001144952.2(SDK2):c.1577C>A (p.Thr526Asn)	rs1105353	0.20896
NM_001144952.2(SDK2):c.1563C>T (p.His521=)	rs1105354	0.20721
NM_001144952.2(SDK2):c.826G>A (p.Gly276Ser)	rs73347768	0.02322
NM_001144952.2(SDK2):c.255C>T (p.His85=)	rs116430423	0.01081

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