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rs121913392

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913392(A;A)
Make rs121913392(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position150054081
GeneCSF1R
is asnp
is mentioned by
dbSNPrs121913392
dbSNP (old)rs121913392
ClinGenrs121913392
ebirs121913392
HLIrs121913392
Exacrs121913392
Gnomadrs121913392
Varsomers121913392
Maprs121913392
PheGenIrs121913392
Biobankrs121913392
1000 genomesrs121913392
hgdprs121913392
ensemblrs121913392
gopubmedrs121913392
geneviewrs121913392
scholarrs121913392
googlers121913392
pharmgkbrs121913392
gwascentralrs121913392
openSNPrs121913392
23andMers121913392
23andMe allrs121913392
SNPshotrs121913392
SNPdbers121913392
MSV3drs121913392
GWAS Ctlgrs121913392
Max Magnitude0
ClinVar
Risk rs121913392(A;A) rs121913392(G;G)
Alt rs121913392(A;A) rs121913392(G;G)
Reference Rs121913392(T;T)
Significance Probable-Pathogenic
Disease Neoplasm
Variation info
Gene CSF1R
CLNDBN Neoplasm
Reversed 1
HGVS NC_000005.9:g.149433644A>C; NC_000005.9:g.149433644A>T
CLNSRC
CLNACC RCV000418290.1, RCV000429439.1,