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rs690016553

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs690016553(C;T)
Make rs690016553(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150054384
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016553
ebirs690016553
HLIrs690016553
Exacrs690016553
Varsomers690016553
Maprs690016553
PheGenIrs690016553
hapmaprs690016553
1000 genomesrs690016553
hgdprs690016553
ensemblrs690016553
gopubmedrs690016553
geneviewrs690016553
scholarrs690016553
googlers690016553
pharmgkbrs690016553
gwascentralrs690016553
openSNPrs690016553
23andMers690016553
23andMe allrs690016553
SNP Nexus

SNPshotrs690016553
SNPdbers690016553
MSV3drs690016553
GWAS Ctlgrs690016553
Max Magnitude0
ClinVar
Risk rs690016553(T;T)
Alt rs690016553(T;T)
Reference rs690016553(C;C)
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.149433947G>A
CLNSRC
CLNACC RCV000149528.1,