Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519802

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519802(G;G)
Make rs1057519802(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position150061765
GeneCSF1R
is asnp
is mentioned by
dbSNPrs1057519802
dbSNP (classic)rs1057519802
ClinGenrs1057519802
ebirs1057519802
HLIrs1057519802
Exacrs1057519802
Gnomadrs1057519802
Varsomers1057519802
LitVarrs1057519802
Maprs1057519802
PheGenIrs1057519802
Biobankrs1057519802
1000 genomesrs1057519802
hgdprs1057519802
ensemblrs1057519802
geneviewrs1057519802
scholarrs1057519802
googlers1057519802
pharmgkbrs1057519802
gwascentralrs1057519802
openSNPrs1057519802
23andMers1057519802
23andMe allrs1057519802
SNPshotrs1057519802
SNPdbers1057519802
MSV3drs1057519802
GWAS Ctlgrs1057519802
Max Magnitude0
ClinVar
Risk rs1057519802(G;G)
Alt rs1057519802(G;G)
Reference Rs1057519802(T;T)
Significance Probable-Pathogenic
Disease Hematologic neoplasm Myeloproliferative disorder
Variation info
Gene CSF1R
CLNDBN Hematologic neoplasm Myeloproliferative disorder
Reversed 1
HGVS NC_000005.9:g.149441328A>C
CLNSRC
CLNACC RCV000430977.1, RCV000440400.1,