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rs690016559

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016559(C;C)
Make rs690016559(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150060874
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016559
ebirs690016559
HLIrs690016559
Exacrs690016559
Varsomers690016559
Maprs690016559
PheGenIrs690016559
hapmaprs690016559
1000 genomesrs690016559
hgdprs690016559
ensemblrs690016559
gopubmedrs690016559
geneviewrs690016559
scholarrs690016559
googlers690016559
pharmgkbrs690016559
gwascentralrs690016559
openSNPrs690016559
23andMers690016559
23andMe allrs690016559
SNP Nexus

SNPshotrs690016559
SNPdbers690016559
MSV3drs690016559
GWAS Ctlgrs690016559
Max Magnitude0
ClinVar
Risk rs690016559(C;C)
Alt rs690016559(C;C)
Reference rs690016559(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.149440437A>G
CLNSRC
CLNACC RCV000149535.1,