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rs690016566

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs690016566(A;A)
Make rs690016566(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150057312
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016566
ebirs690016566
HLIrs690016566
Exacrs690016566
Varsomers690016566
Maprs690016566
PheGenIrs690016566
hapmaprs690016566
1000 genomesrs690016566
hgdprs690016566
ensemblrs690016566
gopubmedrs690016566
geneviewrs690016566
scholarrs690016566
googlers690016566
pharmgkbrs690016566
gwascentralrs690016566
openSNPrs690016566
23andMers690016566
23andMe allrs690016566
SNP Nexus

SNPshotrs690016566
SNPdbers690016566
MSV3drs690016566
GWAS Ctlgrs690016566
Max Magnitude0
ClinVar
Risk rs690016566(A;A)
Alt rs690016566(A;A)
Reference rs690016566(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.149436875C>T
CLNSRC
CLNACC RCV000149542.1,