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rs9430161

From SNPedia

Orientationplus
Stabilizedplus
Make rs9430161(G;G)
Make rs9430161(G;T)
Make rs9430161(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position10986798
GeneLOC390996
is asnp
is mentioned by
dbSNPrs9430161
ebirs9430161
HLIrs9430161
Exacrs9430161
Varsomers9430161
Maprs9430161
PheGenIrs9430161
hapmaprs9430161
1000 genomesrs9430161
hgdprs9430161
ensemblrs9430161
gopubmedrs9430161
geneviewrs9430161
scholarrs9430161
googlers9430161
pharmgkbrs9430161
gwascentralrs9430161
openSNPrs9430161
23andMers9430161
23andMe allrs9430161
SNP Nexus

SNPshotrs9430161
SNPdbers9430161
MSV3drs9430161
GWAS Ctlgrs9430161
GMAF0.2351
Max Magnitude
? (G;G) (G;T) (T;T) 28

[PMID 22327514] Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma