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rs690016557

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs690016557(C;C)
Make rs690016557(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150056068
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016557
ebirs690016557
HLIrs690016557
Exacrs690016557
Varsomers690016557
Maprs690016557
PheGenIrs690016557
hapmaprs690016557
1000 genomesrs690016557
hgdprs690016557
ensemblrs690016557
gopubmedrs690016557
geneviewrs690016557
scholarrs690016557
googlers690016557
pharmgkbrs690016557
gwascentralrs690016557
openSNPrs690016557
23andMers690016557
23andMe allrs690016557
SNP Nexus

SNPshotrs690016557
SNPdbers690016557
MSV3drs690016557
GWAS Ctlgrs690016557
Max Magnitude0
ClinVar
Risk rs690016557(C;C)
Alt rs690016557(C;C)
Reference rs690016557(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.149435631C>G
CLNSRC
CLNACC RCV000149533.1,