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rs121913393

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913393(C;C)
Make rs121913393(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position150054083
GeneCSF1R
is asnp
is mentioned by
dbSNPrs121913393
dbSNP (classic)rs121913393
ClinGenrs121913393
ebirs121913393
HLIrs121913393
Exacrs121913393
Gnomadrs121913393
Varsomers121913393
LitVarrs121913393
Maprs121913393
PheGenIrs121913393
Biobankrs121913393
1000 genomesrs121913393
hgdprs121913393
ensemblrs121913393
geneviewrs121913393
scholarrs121913393
googlers121913393
pharmgkbrs121913393
gwascentralrs121913393
openSNPrs121913393
23andMers121913393
23andMe allrs121913393
SNPshotrs121913393
SNPdbers121913393
MSV3drs121913393
GWAS Ctlgrs121913393
Max Magnitude0
ClinVar
Risk rs121913393(C;C)
Alt rs121913393(C;C)
Reference Rs121913393(T;T)
Significance Probable-Pathogenic
Disease Neoplasm Hematologic neoplasm
Variation info
Gene CSF1R
CLNDBN Neoplasm Hematologic neoplasm
Reversed 1
HGVS NC_000005.9:g.149433646A>G
CLNSRC
CLNACC RCV000423228.1, RCV000434345.1,