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rs690016556

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs690016556(C;T)
Make rs690016556(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150055262
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016556
ebirs690016556
HLIrs690016556
Exacrs690016556
Varsomers690016556
Maprs690016556
PheGenIrs690016556
hapmaprs690016556
1000 genomesrs690016556
hgdprs690016556
ensemblrs690016556
gopubmedrs690016556
geneviewrs690016556
scholarrs690016556
googlers690016556
pharmgkbrs690016556
gwascentralrs690016556
openSNPrs690016556
23andMers690016556
23andMe allrs690016556
SNP Nexus

SNPshotrs690016556
SNPdbers690016556
MSV3drs690016556
GWAS Ctlgrs690016556
Max Magnitude0
ClinVar
Risk rs690016556(T;T)
Alt rs690016556(T;T)
Reference rs690016556(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.149434825G>A
CLNSRC
CLNACC RCV000149532.1,