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rs690016555

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs690016555(A;A)
Make rs690016555(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position150056052
GeneCSF1R
is asnp
is mentioned by
dbSNPrs690016555
ebirs690016555
HLIrs690016555
Exacrs690016555
Varsomers690016555
Maprs690016555
PheGenIrs690016555
hapmaprs690016555
1000 genomesrs690016555
hgdprs690016555
ensemblrs690016555
gopubmedrs690016555
geneviewrs690016555
scholarrs690016555
googlers690016555
pharmgkbrs690016555
gwascentralrs690016555
openSNPrs690016555
23andMers690016555
23andMe allrs690016555
SNP Nexus

SNPshotrs690016555
SNPdbers690016555
MSV3drs690016555
GWAS Ctlgrs690016555
Max Magnitude0
ClinVar
Risk rs690016555(A;A)
Alt rs690016555(A;A)
Reference rs690016555(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.149435615A>T
CLNSRC
CLNACC RCV000149531.1,