Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860277

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860277(C;C)
Make rs281860277(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056034
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860277
ebirs281860277
HLIrs281860277
Exacrs281860277
Varsomers281860277
Maprs281860277
PheGenIrs281860277
hapmaprs281860277
1000 genomesrs281860277
hgdprs281860277
ensemblrs281860277
gopubmedrs281860277
geneviewrs281860277
scholarrs281860277
googlers281860277
pharmgkbrs281860277
gwascentralrs281860277
openSNPrs281860277
23andMers281860277
23andMe allrs281860277
SNP Nexus

SNPshotrs281860277
SNPdbers281860277
MSV3drs281860277
GWAS Ctlgrs281860277
Max Magnitude0
ClinVar
Risk rs281860277(C;C)
Alt rs281860277(C;C)
Reference rs281860277(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.149435597A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000031934.1,