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rs281860280

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860280(A;A)
Make rs281860280(A;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position150055259
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860280
ebirs281860280
HLIrs281860280
Exacrs281860280
Varsomers281860280
Maprs281860280
PheGenIrs281860280
hapmaprs281860280
1000 genomesrs281860280
hgdprs281860280
ensemblrs281860280
gopubmedrs281860280
geneviewrs281860280
scholarrs281860280
googlers281860280
pharmgkbrs281860280
gwascentralrs281860280
openSNPrs281860280
23andMers281860280
23andMe allrs281860280
SNP Nexus

SNPshotrs281860280
SNPdbers281860280
MSV3drs281860280
GWAS Ctlgrs281860280
Max Magnitude0
ClinVar
Risk rs281860280(A;A)
Alt rs281860280(A;A)
Reference rs281860280(C;C)
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.149434822G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000031937.1,