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rs281860273

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860273(A;A)
Make rs281860273(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056337
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860273
ebirs281860273
HLIrs281860273
Exacrs281860273
Varsomers281860273
Maprs281860273
PheGenIrs281860273
hapmaprs281860273
1000 genomesrs281860273
hgdprs281860273
ensemblrs281860273
gopubmedrs281860273
geneviewrs281860273
scholarrs281860273
googlers281860273
pharmgkbrs281860273
gwascentralrs281860273
openSNPrs281860273
23andMers281860273
23andMe allrs281860273
SNP Nexus

SNPshotrs281860273
SNPdbers281860273
MSV3drs281860273
GWAS Ctlgrs281860273
Max Magnitude0
ClinVar
Risk rs281860273(A;A)
Alt rs281860273(A;A)
Reference rs281860273(T;T)
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.149435900A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031931.1,