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

rs281860270

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860270(C;C)
Make rs281860270(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150057309
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860270
ebirs281860270
HLIrs281860270
Exacrs281860270
Varsomers281860270
Maprs281860270
PheGenIrs281860270
hapmaprs281860270
1000 genomesrs281860270
hgdprs281860270
ensemblrs281860270
gopubmedrs281860270
geneviewrs281860270
scholarrs281860270
googlers281860270
pharmgkbrs281860270
gwascentralrs281860270
openSNPrs281860270
23andMers281860270
23andMe allrs281860270
SNP Nexus

SNPshotrs281860270
SNPdbers281860270
MSV3drs281860270
GWAS Ctlgrs281860270
Max Magnitude0
ClinVar
Risk rs281860270(C;C)
Alt rs281860270(C;C)
Reference rs281860270(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.149436872A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000031928.1,