List of variants in gene CSF1R reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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_001288705.3(CSF1R):c.84T>C (p.Pro28=)	rs216123	0.46517
NM_001288705.3(CSF1R):c.1626+7C>T	rs34928010	0.13020
NM_001288705.3(CSF1R):c.1085A>G (p.His362Arg)	rs10079250	0.08472
NM_001288705.3(CSF1R):c.294C>T (p.His98=)	rs17652007	0.03331
NM_001288705.3(CSF1R):c.2535C>G (p.Leu845=)	rs56327604	0.03157
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.282C>T (p.Ser94=)	rs41287102	0.00495
NM_001288705.3(CSF1R):c.95T>G (p.Val32Gly)	rs56048668	0.00332
NM_001288705.3(CSF1R):c.2799T>C (p.Gly933=)	rs41287092	0.00258

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