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rs690016549

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016549(C;C)
Make rs690016549(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150056130
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016549
ebirs690016549
HLIrs690016549
Exacrs690016549
Varsomers690016549
Maprs690016549
PheGenIrs690016549
hapmaprs690016549
1000 genomesrs690016549
hgdprs690016549
ensemblrs690016549
gopubmedrs690016549
geneviewrs690016549
scholarrs690016549
googlers690016549
pharmgkbrs690016549
gwascentralrs690016549
openSNPrs690016549
23andMers690016549
23andMe allrs690016549
SNP Nexus

SNPshotrs690016549
SNPdbers690016549
MSV3drs690016549
GWAS Ctlgrs690016549
Max Magnitude0
ClinVar
Risk rs690016549(C;C)
Alt rs690016549(C;C)
Reference rs690016549(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.149435693A>G
CLNSRC
CLNACC RCV000149524.1,