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rs16863886

From SNPedia

Orientationplus
Stabilizedplus
Make rs16863886(C;C)
Make rs16863886(C;T)
Make rs16863886(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position222567378
is asnp
is mentioned by
dbSNPrs16863886
ebirs16863886
HLIrs16863886
Exacrs16863886
Varsomers16863886
Maprs16863886
PheGenIrs16863886
hapmaprs16863886
1000 genomesrs16863886
hgdprs16863886
ensemblrs16863886
gopubmedrs16863886
geneviewrs16863886
scholarrs16863886
googlers16863886
pharmgkbrs16863886
gwascentralrs16863886
openSNPrs16863886
23andMers16863886
23andMe allrs16863886
SNP Nexus

SNPshotrs16863886
SNPdbers16863886
MSV3drs16863886
GWAS Ctlgrs16863886
GMAF0.2746
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 21596488] Use of Germline Polymorphisms in Predicting Concurrent Chemoradiotherapy Response in Esophageal Cancer