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rs397515557

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515557(C;C)
Make rs397515557(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056097
GeneCSF1R
is asnp
is mentioned by
dbSNPrs397515557
ebirs397515557
HLIrs397515557
Exacrs397515557
Varsomers397515557
Maprs397515557
PheGenIrs397515557
hapmaprs397515557
1000 genomesrs397515557
hgdprs397515557
ensemblrs397515557
gopubmedrs397515557
geneviewrs397515557
scholarrs397515557
googlers397515557
pharmgkbrs397515557
gwascentralrs397515557
openSNPrs397515557
23andMers397515557
23andMe allrs397515557
SNP Nexus

SNPshotrs397515557
SNPdbers397515557
MSV3drs397515557
GWAS Ctlgrs397515557
Max Magnitude0
ClinVar
Risk rs397515557(C;C)
Alt rs397515557(C;C)
Reference rs397515557(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.149435660A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000055912.1,