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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
ebirs11590362
HLIrs11590362
Exacrs11590362
Varsomers11590362
Maprs11590362
PheGenIrs11590362
hapmaprs11590362
1000 genomesrs11590362
hgdprs11590362
ensemblrs11590362
gopubmedrs11590362
geneviewrs11590362
scholarrs11590362
googlers11590362
pharmgkbrs11590362
gwascentralrs11590362
openSNPrs11590362
23andMers11590362
23andMe allrs11590362
SNP Nexus

SNPshotrs11590362
SNPdbers11590362
MSV3drs11590362
GWAS Ctlgrs11590362
Max Magnitude
? (A;A) (A;G) (G;G) 28

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