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rs10766117

From SNPedia

Orientationplus
Stabilizedplus
Make rs10766117(G;G)
Make rs10766117(G;T)
Make rs10766117(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position13874030
GeneLOC105376561
is asnp
is mentioned by
dbSNPrs10766117
dbSNP (classic)rs10766117
ClinGenrs10766117
ebirs10766117
HLIrs10766117
Exacrs10766117
Gnomadrs10766117
Varsomers10766117
LitVarrs10766117
Maprs10766117
PheGenIrs10766117
Biobankrs10766117
1000 genomesrs10766117
hgdprs10766117
ensemblrs10766117
geneviewrs10766117
scholarrs10766117
googlers10766117
pharmgkbrs10766117
gwascentralrs10766117
openSNPrs10766117
23andMers10766117
SNPshotrs10766117
SNPdbers10766117
MSV3drs10766117
GWAS Ctlgrs10766117
Max Magnitude0
? (G;G) (G;T) (T;T) 28


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