List of variants in gene SAMD9 reported as benign by Genetic Services Laboratory, University of Chicago

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_017654.4(SAMD9):c.4733T>C (p.Ile1578Thr)	rs144380633	0.00599
NM_017654.4(SAMD9):c.1347T>C (p.Asn449=)	rs150107667	0.00542
NM_017654.4(SAMD9):c.1398A>C (p.Pro466=)	rs138066899	0.00533
NM_017654.4(SAMD9):c.4666G>A (p.Ala1556Thr)	rs34896991	0.00462
NM_017654.4(SAMD9):c.257C>T (p.Ser86Phe)	rs147157740	0.00428
NM_017654.4(SAMD9):c.1920C>T (p.Val640=)	rs115425131	0.00377
NM_017654.4(SAMD9):c.4561G>A (p.Glu1521Lys)	rs115350620	0.00320
NM_017654.4(SAMD9):c.4102G>A (p.Glu1368Lys)	rs138600971	0.00149
NM_017654.4(SAMD9):c.1860A>G (p.Lys620=)	rs77922936	0.00078
NM_017654.4(SAMD9):c.3651dup (p.Asp1218Ter)	rs199887936

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