List of variants in gene SDK2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001144952.2(SDK2):c.648C>G (p.Thr216=)	rs61752534	0.00611
NM_001144952.2(SDK2):c.5136C>T (p.Ser1712=)	rs139535646	0.00365
NM_001144952.2(SDK2):c.5997C>T (p.Ser1999=)	rs138003419	0.00004
NM_001144952.2(SDK2):c.2907C>T (p.Ala969=)	rs143289914	0.00002
NM_001144952.2(SDK2):c.6372C>A (p.Gly2124=)	rs982092760	0.00002
NM_001144952.2(SDK2):c.1640G>T (p.Arg547Leu)	rs35867741
NM_001144952.2(SDK2):c.1833G>A (p.Thr611=)	rs146912233
NM_001144952.2(SDK2):c.2448C>A (p.Ser816Arg)	rs143251430
NM_001144952.2(SDK2):c.4218G>A (p.Pro1406=)	rs147384840

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