Have questions? Visit https://www.reddit.com/r/SNPedia

rs1237485

From SNPedia

Orientationminus
Stabilizedminus
Make rs1237485(C;C)
Make rs1237485(C;T)
Make rs1237485(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position28926567
is asnp
is mentioned by
dbSNPrs1237485
dbSNP (classic)rs1237485
ClinGenrs1237485
ebirs1237485
HLIrs1237485
Exacrs1237485
Gnomadrs1237485
Varsomers1237485
LitVarrs1237485
Maprs1237485
PheGenIrs1237485
Biobankrs1237485
1000 genomesrs1237485
hgdprs1237485
ensemblrs1237485
geneviewrs1237485
scholarrs1237485
googlers1237485
pharmgkbrs1237485
gwascentralrs1237485
openSNPrs1237485
23andMers1237485
SNPshotrs1237485
SNPdbers1237485
MSV3drs1237485
GWAS Ctlgrs1237485
GMAF0.3586
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 23991122OA-icon.png] SNP Association Mapping across the Extended Major Histocompatibility Complex and Risk of B-Cell Precursor Acute Lymphoblastic Leukemia in Children