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rs690016547

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016547(G;G)
Make rs690016547(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150060942
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016547
ebirs690016547
HLIrs690016547
Exacrs690016547
Varsomers690016547
Maprs690016547
PheGenIrs690016547
hapmaprs690016547
1000 genomesrs690016547
hgdprs690016547
ensemblrs690016547
gopubmedrs690016547
geneviewrs690016547
scholarrs690016547
googlers690016547
pharmgkbrs690016547
gwascentralrs690016547
openSNPrs690016547
23andMers690016547
23andMe allrs690016547
SNP Nexus

SNPshotrs690016547
SNPdbers690016547
MSV3drs690016547
GWAS Ctlgrs690016547
Max Magnitude0
ClinVar
Risk rs690016547(G;G)
Alt rs690016547(G;G)
Reference rs690016547(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.149440505A>C
CLNSRC
CLNACC RCV000149522.1,