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rs690016565

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016565(A;A)
Make rs690016565(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150055329
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016565
ebirs690016565
HLIrs690016565
Exacrs690016565
Varsomers690016565
Maprs690016565
PheGenIrs690016565
hapmaprs690016565
1000 genomesrs690016565
hgdprs690016565
ensemblrs690016565
gopubmedrs690016565
geneviewrs690016565
scholarrs690016565
googlers690016565
pharmgkbrs690016565
gwascentralrs690016565
openSNPrs690016565
23andMers690016565
23andMe allrs690016565
SNP Nexus

SNPshotrs690016565
SNPdbers690016565
MSV3drs690016565
GWAS Ctlgrs690016565
Max Magnitude0
ClinVar
Risk rs690016565(A;A)
Alt rs690016565(A;A)
Reference rs690016565(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.149434892A>T
CLNSRC
CLNACC RCV000149541.1,