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rs690016551

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs690016551(C;C)
Make rs690016551(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150056039
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016551
ebirs690016551
HLIrs690016551
Exacrs690016551
Varsomers690016551
Maprs690016551
PheGenIrs690016551
hapmaprs690016551
1000 genomesrs690016551
hgdprs690016551
ensemblrs690016551
gopubmedrs690016551
geneviewrs690016551
scholarrs690016551
googlers690016551
pharmgkbrs690016551
gwascentralrs690016551
openSNPrs690016551
23andMers690016551
23andMe allrs690016551
SNP Nexus

SNPshotrs690016551
SNPdbers690016551
MSV3drs690016551
GWAS Ctlgrs690016551
Max Magnitude0
ClinVar
Risk rs690016551(C;C)
Alt rs690016551(C;C)
Reference rs690016551(G;G)
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.149435602C>G
CLNSRC
CLNACC RCV000149526.1,