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rs281860268

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860268(A;A)
Make rs281860268(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150061583
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860268
ebirs281860268
HLIrs281860268
Exacrs281860268
Varsomers281860268
Maprs281860268
PheGenIrs281860268
hapmaprs281860268
1000 genomesrs281860268
hgdprs281860268
ensemblrs281860268
gopubmedrs281860268
geneviewrs281860268
scholarrs281860268
googlers281860268
pharmgkbrs281860268
gwascentralrs281860268
openSNPrs281860268
23andMers281860268
23andMe allrs281860268
SNP Nexus

SNPshotrs281860268
SNPdbers281860268
MSV3drs281860268
GWAS Ctlgrs281860268
Max Magnitude0
ClinVar
Risk rs281860268(A;A)
Alt rs281860268(A;A)
Reference rs281860268(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.149441146C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031927.1,