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rs1052667

From SNPedia

Orientationplus
Stabilizedplus
Make rs1052667(C;C)
Make rs1052667(C;T)
Make rs1052667(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position47004177
GeneARHGAP35
is asnp
is mentioned by
dbSNPrs1052667
dbSNP (classic)rs1052667
ClinGenrs1052667
ebirs1052667
HLIrs1052667
Exacrs1052667
Gnomadrs1052667
Varsomers1052667
LitVarrs1052667
Maprs1052667
PheGenIrs1052667
Biobankrs1052667
1000 genomesrs1052667
hgdprs1052667
ensemblrs1052667
geneviewrs1052667
scholarrs1052667
googlers1052667
pharmgkbrs1052667
gwascentralrs1052667
openSNPrs1052667
23andMers1052667
SNPshotrs1052667
SNPdbers1052667
MSV3drs1052667
GWAS Ctlgrs1052667
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25136583OA-icon.png] Rho GTPase-Activating Protein 35 rs1052667 Polymorphism and Osteosarcoma Risk and Prognosis