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rs11590362

From SNPedia

Orientationplus
Stabilizedplus
Make rs11590362(A;A)
Make rs11590362(A;G)
Make rs11590362(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position42742890
is asnp
is mentioned by
dbSNPrs11590362
dbSNP (classic)rs11590362
ClinGenrs11590362
ebirs11590362
HLIrs11590362
Exacrs11590362
Gnomadrs11590362
Varsomers11590362
LitVarrs11590362
Maprs11590362
PheGenIrs11590362
Biobankrs11590362
1000 genomesrs11590362
hgdprs11590362
ensemblrs11590362
geneviewrs11590362
scholarrs11590362
googlers11590362
pharmgkbrs11590362
gwascentralrs11590362
openSNPrs11590362
23andMers11590362
SNPshotrs11590362
SNPdbers11590362
MSV3drs11590362
GWAS Ctlgrs11590362
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 25733456OA-icon.png] Genetic Variations in Magnesium-Related Ion Channels May Affect Diabetes Risk among African American and Hispanic American Women