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rs281860275

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860275(C;C)
Make rs281860275(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056214
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860275
ebirs281860275
HLIrs281860275
Exacrs281860275
Varsomers281860275
Maprs281860275
PheGenIrs281860275
hapmaprs281860275
1000 genomesrs281860275
hgdprs281860275
ensemblrs281860275
gopubmedrs281860275
geneviewrs281860275
scholarrs281860275
googlers281860275
pharmgkbrs281860275
gwascentralrs281860275
openSNPrs281860275
23andMers281860275
23andMe allrs281860275
SNP Nexus

SNPshotrs281860275
SNPdbers281860275
MSV3drs281860275
GWAS Ctlgrs281860275
Max Magnitude0
ClinVar
Risk rs281860275(C;C)
Alt rs281860275(C;C)
Reference rs281860275(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.149435777C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000031933.1,