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rs397515555

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515555(A;A)
Make rs397515555(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150060873
GeneCSF1R
is asnp
is mentioned by
dbSNPrs397515555
ebirs397515555
HLIrs397515555
Exacrs397515555
Varsomers397515555
Maprs397515555
PheGenIrs397515555
hapmaprs397515555
1000 genomesrs397515555
hgdprs397515555
ensemblrs397515555
gopubmedrs397515555
geneviewrs397515555
scholarrs397515555
googlers397515555
pharmgkbrs397515555
gwascentralrs397515555
openSNPrs397515555
23andMers397515555
23andMe allrs397515555
SNP Nexus

SNPshotrs397515555
SNPdbers397515555
MSV3drs397515555
GWAS Ctlgrs397515555
Max Magnitude0
ClinVar
Risk rs397515555(A;A)
Alt rs397515555(A;A)
Reference rs397515555(G;G)
Significance Pathogenic
Disease Hereditary diffuse leukoencephalopathy with spheroids
Variation info
Gene CSF1R
CLNDBN Hereditary diffuse leukoencephalopathy with spheroids
Reversed 1
HGVS NC_000005.9:g.149440436C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000055910.1,