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rs281860272

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860272(A;G)
Make rs281860272(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056343
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860272
ebirs281860272
HLIrs281860272
Exacrs281860272
Varsomers281860272
Maprs281860272
PheGenIrs281860272
hapmaprs281860272
1000 genomesrs281860272
hgdprs281860272
ensemblrs281860272
gopubmedrs281860272
geneviewrs281860272
scholarrs281860272
googlers281860272
pharmgkbrs281860272
gwascentralrs281860272
openSNPrs281860272
23andMers281860272
23andMe allrs281860272
SNP Nexus

SNPshotrs281860272
SNPdbers281860272
MSV3drs281860272
GWAS Ctlgrs281860272
Max Magnitude0
ClinVar
Risk rs281860272(G;G)
Alt rs281860272(G;G)
Reference rs281860272(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.149435906T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000031930.1,