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rs281860279

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860279(C;C)
Make rs281860279(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150055267
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860279
ebirs281860279
HLIrs281860279
Exacrs281860279
Varsomers281860279
Maprs281860279
PheGenIrs281860279
hapmaprs281860279
1000 genomesrs281860279
hgdprs281860279
ensemblrs281860279
gopubmedrs281860279
geneviewrs281860279
scholarrs281860279
googlers281860279
pharmgkbrs281860279
gwascentralrs281860279
openSNPrs281860279
23andMers281860279
23andMe allrs281860279
SNP Nexus

SNPshotrs281860279
SNPdbers281860279
MSV3drs281860279
GWAS Ctlgrs281860279
Max Magnitude0
ClinVar
Risk rs281860279(C;C)
Alt rs281860279(C;C)
Reference rs281860279(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.149434830A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000022684.27,