List of variants in gene CSF1R reported as 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001288705.3(CSF1R):c.1237G>A (p.Gly413Ser)	rs34951517	0.00996
NM_001288705.3(CSF1R):c.2709C>T (p.Phe903=)	rs41287094	0.00742
NM_001288705.3(CSF1R):c.2799T>C (p.Gly933=)	rs41287092	0.00258
NM_001288705.3(CSF1R):c.835G>A (p.Val279Met)	rs3829986	0.00089

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