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rs9784100

From SNPedia

Orientationplus
Stabilizedplus
Make rs9784100(C;C)
Make rs9784100(C;G)
Make rs9784100(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position60335579
is asnp
is mentioned by
dbSNPrs9784100
ebirs9784100
HLIrs9784100
Exacrs9784100
Varsomers9784100
Maprs9784100
PheGenIrs9784100
hapmaprs9784100
1000 genomesrs9784100
hgdprs9784100
ensemblrs9784100
gopubmedrs9784100
geneviewrs9784100
scholarrs9784100
googlers9784100
pharmgkbrs9784100
gwascentralrs9784100
openSNPrs9784100
23andMers9784100
23andMe allrs9784100
SNP Nexus

SNPshotrs9784100
SNPdbers9784100
MSV3drs9784100
GWAS Ctlgrs9784100
GMAF0.3067
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 22318908OA-icon.png] Genetic variants within ultraconserved elements and susceptibility to right- and left-sided colorectal adenocarcinoma