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rs690016560

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016560(C;C)
Make rs690016560(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150054368
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016560
ebirs690016560
HLIrs690016560
Exacrs690016560
Varsomers690016560
Maprs690016560
PheGenIrs690016560
hapmaprs690016560
1000 genomesrs690016560
hgdprs690016560
ensemblrs690016560
gopubmedrs690016560
geneviewrs690016560
scholarrs690016560
googlers690016560
pharmgkbrs690016560
gwascentralrs690016560
openSNPrs690016560
23andMers690016560
23andMe allrs690016560
SNP Nexus

SNPshotrs690016560
SNPdbers690016560
MSV3drs690016560
GWAS Ctlgrs690016560
Max Magnitude0
ClinVar
Risk rs690016560(C;C)
Alt rs690016560(C;C)
Reference rs690016560(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.149433931A>G
CLNSRC
CLNACC RCV000149536.1,