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rs1399685

From SNPedia

Orientationplus
Stabilizedplus
Make rs1399685(A;A)
Make rs1399685(A;T)
Make rs1399685(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position146870842
is asnp
is mentioned by
dbSNPrs1399685
ebirs1399685
HLIrs1399685
Exacrs1399685
Varsomers1399685
Maprs1399685
PheGenIrs1399685
hapmaprs1399685
1000 genomesrs1399685
hgdprs1399685
ensemblrs1399685
gopubmedrs1399685
geneviewrs1399685
scholarrs1399685
googlers1399685
pharmgkbrs1399685
gwascentralrs1399685
openSNPrs1399685
23andMers1399685
23andMe allrs1399685
SNP Nexus

SNPshotrs1399685
SNPdbers1399685
MSV3drs1399685
GWAS Ctlgrs1399685
GMAF0.02158
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 22318908OA-icon.png] Genetic variants within ultraconserved elements and susceptibility to right- and left-sided colorectal adenocarcinoma