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rs1057520014

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520014(G;T)
Make rs1057520014(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position150073480
GeneCSF1R
is asnp
is mentioned by
dbSNPrs1057520014
dbSNP (classic)rs1057520014
ClinGenrs1057520014
ebirs1057520014
HLIrs1057520014
Exacrs1057520014
Gnomadrs1057520014
Varsomers1057520014
LitVarrs1057520014
Maprs1057520014
PheGenIrs1057520014
Biobankrs1057520014
1000 genomesrs1057520014
hgdprs1057520014
ensemblrs1057520014
geneviewrs1057520014
scholarrs1057520014
googlers1057520014
pharmgkbrs1057520014
gwascentralrs1057520014
openSNPrs1057520014
23andMers1057520014
SNPshotrs1057520014
SNPdbers1057520014
MSV3drs1057520014
GWAS Ctlgrs1057520014
Max Magnitude0
ClinVar
Risk rs1057520014(T;T)
Alt rs1057520014(T;T)
Reference Rs1057520014(G;G)
Significance Probable-Pathogenic
Disease Hematologic neoplasm
Variation info
Gene CSF1R
CLNDBN Hematologic neoplasm
Reversed 1
HGVS NC_000005.9:g.149453043C>A
CLNSRC
CLNACC RCV000432996.1,