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rs281860271

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860271(C;C)
Make rs281860271(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150057298
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860271
ebirs281860271
HLIrs281860271
Exacrs281860271
Varsomers281860271
Maprs281860271
PheGenIrs281860271
hapmaprs281860271
1000 genomesrs281860271
hgdprs281860271
ensemblrs281860271
gopubmedrs281860271
geneviewrs281860271
scholarrs281860271
googlers281860271
pharmgkbrs281860271
gwascentralrs281860271
openSNPrs281860271
23andMers281860271
23andMe allrs281860271
SNP Nexus

SNPshotrs281860271
SNPdbers281860271
MSV3drs281860271
GWAS Ctlgrs281860271
Max Magnitude0
ClinVar
Risk rs281860271(A,C;A,C)
Alt rs281860271(A,C;A,C)
Reference rs281860271(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.149436861C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000031929.1,