Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs121913390

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913390(A;A)
Make rs121913390(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position150073481
GeneCSF1R
is asnp
is mentioned by
dbSNPrs121913390
dbSNP (old)rs121913390
ClinGenrs121913390
ebirs121913390
HLIrs121913390
Exacrs121913390
Gnomadrs121913390
Varsomers121913390
Maprs121913390
PheGenIrs121913390
Biobankrs121913390
1000 genomesrs121913390
hgdprs121913390
ensemblrs121913390
gopubmedrs121913390
geneviewrs121913390
scholarrs121913390
googlers121913390
pharmgkbrs121913390
gwascentralrs121913390
openSNPrs121913390
23andMers121913390
23andMe allrs121913390
SNPshotrs121913390
SNPdbers121913390
MSV3drs121913390
GWAS Ctlgrs121913390
Max Magnitude0
ClinVar
Risk rs121913390(A;A) rs121913390(C;C)
Alt rs121913390(A;A) rs121913390(C;C)
Reference Rs121913390(T;T)
Significance Probable-Pathogenic
Disease Neoplasm Hematologic neoplasm
Variation info
Gene CSF1R
CLNDBN Neoplasm Hematologic neoplasm
Reversed 1
HGVS NC_000005.9:g.149453044A>G; NC_000005.9:g.149453044A>T
CLNSRC
CLNACC RCV000424293.1, RCV000441113.1, RCV000434527.1,