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rs587777245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777245(-;-)
Make rs587777245(-;A)
Make rs587777245(A;A)
ReferenceGRCh38 38.1/142
Chromosome5
Position150059772
GeneCSF1R
is asnp
is mentioned by
dbSNPrs587777245
ebirs587777245
HLIrs587777245
Exacrs587777245
Varsomers587777245
Maprs587777245
PheGenIrs587777245
hapmaprs587777245
1000 genomesrs587777245
hgdprs587777245
ensemblrs587777245
gopubmedrs587777245
geneviewrs587777245
scholarrs587777245
googlers587777245
pharmgkbrs587777245
gwascentralrs587777245
openSNPrs587777245
23andMers587777245
23andMe allrs587777245
SNP Nexus

SNPshotrs587777245
SNPdbers587777245
MSV3drs587777245
GWAS Ctlgrs587777245
Max Magnitude0
ClinVar
Risk rs587777245(A;A)
Alt rs587777245(A;A)
Reference rs587777245(;)
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.149439335dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000106403.3,