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

rs281860269

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860269(A;A)
Make rs281860269(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150060934
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860269
ebirs281860269
HLIrs281860269
Exacrs281860269
Varsomers281860269
Maprs281860269
PheGenIrs281860269
hapmaprs281860269
1000 genomesrs281860269
hgdprs281860269
ensemblrs281860269
gopubmedrs281860269
geneviewrs281860269
scholarrs281860269
googlers281860269
pharmgkbrs281860269
gwascentralrs281860269
openSNPrs281860269
23andMers281860269
23andMe allrs281860269
SNP Nexus

SNPshotrs281860269
SNPdbers281860269
MSV3drs281860269
GWAS Ctlgrs281860269
Max Magnitude0
ClinVar
Risk rs281860269(A;A)
Alt rs281860269(A;A)
Reference rs281860269(G;G)
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.149440497C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000022685.27,