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rs281860276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Make rs281860276(-;-)
Make rs281860276(-;TCT)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056032
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860276
ebirs281860276
HLIrs281860276
Exacrs281860276
Varsomers281860276
Maprs281860276
PheGenIrs281860276
hapmaprs281860276
1000 genomesrs281860276
hgdprs281860276
ensemblrs281860276
gopubmedrs281860276
geneviewrs281860276
scholarrs281860276
googlers281860276
pharmgkbrs281860276
gwascentralrs281860276
openSNPrs281860276
23andMers281860276
23andMe allrs281860276
SNP Nexus

SNPshotrs281860276
SNPdbers281860276
MSV3drs281860276
GWAS Ctlgrs281860276
Max Magnitude0
ClinVar
Risk rs281860276(;)
Alt rs281860276(;)
Reference rs281860276(TCT;TCT)
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.149435595_149435597delAGA
CLNSRC ClinVar GeneReviews
CLNACC RCV000031935.1,