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rs387906662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906662(G;T)
Make rs387906662(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056071
GeneCSF1R
is asnp
is mentioned by
dbSNPrs387906662
ebirs387906662
HLIrs387906662
Exacrs387906662
Varsomers387906662
Maprs387906662
PheGenIrs387906662
hapmaprs387906662
1000 genomesrs387906662
hgdprs387906662
ensemblrs387906662
gopubmedrs387906662
geneviewrs387906662
scholarrs387906662
googlers387906662
pharmgkbrs387906662
gwascentralrs387906662
openSNPrs387906662
23andMers387906662
23andMe allrs387906662
SNP Nexus

SNPshotrs387906662
SNPdbers387906662
MSV3drs387906662
GWAS Ctlgrs387906662
Max Magnitude0
ClinVar
Risk rs387906662(T;T)
Alt rs387906662(T;T)
Reference rs387906662(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.149435634C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022688.27,