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rs10079250

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs10079250(C;C)
Make rs10079250(C;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position150070569
GeneCSF1R
is asnp
is mentioned by
dbSNPrs10079250
dbSNP (old)rs10079250
ClinGenrs10079250
ebirs10079250
HLIrs10079250
Exacrs10079250
Gnomadrs10079250
Varsomers10079250
Maprs10079250
PheGenIrs10079250
Biobankrs10079250
1000 genomesrs10079250
hgdprs10079250
ensemblrs10079250
gopubmedrs10079250
geneviewrs10079250
scholarrs10079250
googlers10079250
pharmgkbrs10079250
gwascentralrs10079250
openSNPrs10079250
23andMers10079250
23andMe allrs10079250
SNP Nexus

SNPshotrs10079250
SNPdbers10079250
MSV3drs10079250
GWAS Ctlgrs10079250
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 25144241] A Functional Polymorphism in CSF1R Gene Is a Novel Susceptibility Marker for Lung Cancer among Never-Smoking Females


ClinVar
Risk rs10079250(C;C)
Alt rs10079250(C;C)
Reference Rs10079250(T;T)
Significance Non-pathogenic
Disease Hereditary diffuse leukoencephalopathy with spheroids
Variation info
Gene CSF1R
CLNDBN Hereditary diffuse leukoencephalopathy with spheroids
Reversed 0
HGVS NC_000005.9:g.149450132T>C
CLNSRC
CLNACC RCV000280124.1,