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rs281860281

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860281(A;A)
Make rs281860281(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position150056316
GeneCSF1R
is asnp
is mentioned by
dbSNPrs281860281
ebirs281860281
HLIrs281860281
Exacrs281860281
Varsomers281860281
Maprs281860281
PheGenIrs281860281
hapmaprs281860281
1000 genomesrs281860281
hgdprs281860281
ensemblrs281860281
gopubmedrs281860281
geneviewrs281860281
scholarrs281860281
googlers281860281
pharmgkbrs281860281
gwascentralrs281860281
openSNPrs281860281
23andMers281860281
23andMe allrs281860281
SNP Nexus

SNPshotrs281860281
SNPdbers281860281
MSV3drs281860281
GWAS Ctlgrs281860281
Max Magnitude0
ClinVar
Risk rs281860281(A;A)
Alt rs281860281(A;A)
Reference rs281860281(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.149435879C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000031932.4,