Have questions? Visit https://www.reddit.com/r/SNPedia

rs690016552

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016552(C;C)
Make rs690016552(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150055325
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016552
ebirs690016552
HLIrs690016552
Exacrs690016552
Varsomers690016552
Maprs690016552
PheGenIrs690016552
hapmaprs690016552
1000 genomesrs690016552
hgdprs690016552
ensemblrs690016552
gopubmedrs690016552
geneviewrs690016552
scholarrs690016552
googlers690016552
pharmgkbrs690016552
gwascentralrs690016552
openSNPrs690016552
23andMers690016552
23andMe allrs690016552
SNP Nexus

SNPshotrs690016552
SNPdbers690016552
MSV3drs690016552
GWAS Ctlgrs690016552
Max Magnitude0
ClinVar
Risk rs690016552(C;C)
Alt rs690016552(C;C)
Reference rs690016552(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.149434888A>G
CLNSRC
CLNACC RCV000149527.1,