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

rs587777247

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777247(G;T)
Make rs587777247(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position150056319
GeneCSF1R
is asnp
is mentioned by
dbSNPrs587777247
ebirs587777247
HLIrs587777247
Exacrs587777247
Varsomers587777247
Maprs587777247
PheGenIrs587777247
hapmaprs587777247
1000 genomesrs587777247
hgdprs587777247
ensemblrs587777247
gopubmedrs587777247
geneviewrs587777247
scholarrs587777247
googlers587777247
pharmgkbrs587777247
gwascentralrs587777247
openSNPrs587777247
23andMers587777247
23andMe allrs587777247
SNP Nexus

SNPshotrs587777247
SNPdbers587777247
MSV3drs587777247
GWAS Ctlgrs587777247
Max Magnitude0
ClinVar
Risk rs587777247(A,T;A,T)
Alt rs587777247(A,T;A,T)
Reference rs587777247(G;G)
Significance Pathogenic
Disease Hereditary diffuse leukoencephalopathy with spheroids
Variation info
Gene CSF1R
CLNDBN Hereditary diffuse leukoencephalopathy with spheroids
Reversed 0
HGVS NC_000005.9:g.149435882G>A; NC_000005.9:g.149435882G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000149530.2, RCV000106405.3,