"Genome-Nilou Lab"[submitter] AND "CSF1R"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 352120	NM_001288705.3(CSF1R):c.*36A>C	CSF1R	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +2 more	GBenign
Select item 352121	NM_001288705.3(CSF1R):c.*35C>T	CSF1R	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +2 more	GBenign
Select item 1255410	NM_001288705.3(CSF1R):c.2442+23C>T	CSF1R	Single nucleotide variant (intron variant)	Hereditary diffuse leukoencephalopathy with spheroids +2 more	GBenign
Select item 1236822	NM_001288705.3(CSF1R):c.2133-35G>C	CSF1R	Single nucleotide variant (intron variant)	Hereditary diffuse leukoencephalopathy with spheroids +2 more	GBenign
Select item 352165	NM_001288705.3(CSF1R):c.726C>T (p.Thr242=)	CSF1R, LOC111188154	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse leukoencephalopathy with spheroids +2 more	GBenign
Select item 352179	NM_001288705.3(CSF1R):c.84T>C (p.Pro28=)	CSF1R	Single nucleotide variant (synonymous variant +2 more)	Brain abnormalities, neurodegeneration, and dysosteosclerosis +2 more	GBenign

ClinVar