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rs281860267

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860267(A;G)
Make rs281860267(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150061597
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860267
ebirs281860267
HLIrs281860267
Exacrs281860267
Varsomers281860267
Maprs281860267
PheGenIrs281860267
hapmaprs281860267
1000 genomesrs281860267
hgdprs281860267
ensemblrs281860267
gopubmedrs281860267
geneviewrs281860267
scholarrs281860267
googlers281860267
pharmgkbrs281860267
gwascentralrs281860267
openSNPrs281860267
23andMers281860267
23andMe allrs281860267
SNP Nexus

SNPshotrs281860267
SNPdbers281860267
MSV3drs281860267
GWAS Ctlgrs281860267
Max Magnitude0
ClinVar
Risk rs281860267(G;G)
Alt rs281860267(G;G)
Reference rs281860267(A;A)
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.149441160T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022686.27,