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rs16983007

From SNPedia

Orientationplus
Stabilizedplus
Make rs16983007(C;C)
Make rs16983007(C;T)
Make rs16983007(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position24351161
is asnp
is mentioned by
dbSNPrs16983007
dbSNP (classic)rs16983007
ClinGenrs16983007
ebirs16983007
HLIrs16983007
Exacrs16983007
Gnomadrs16983007
Varsomers16983007
LitVarrs16983007
Maprs16983007
PheGenIrs16983007
Biobankrs16983007
1000 genomesrs16983007
hgdprs16983007
ensemblrs16983007
geneviewrs16983007
scholarrs16983007
googlers16983007
pharmgkbrs16983007
gwascentralrs16983007
openSNPrs16983007
23andMers16983007
SNPshotrs16983007
SNPdbers16983007
MSV3drs16983007
GWAS Ctlgrs16983007
GMAF0.1499
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 22673945OA-icon.png] Identification of polymorphisms in ultraconserved elements associated with clinical outcomes in locally advanced colorectal adenocarcinoma