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rs5929706

From SNPedia

Orientationplus
Stabilizedplus
Make rs5929706(A;A)
Make rs5929706(A;C)
Make rs5929706(C;C)
ReferenceGRCh38 38.1/142
ChromosomeX
Position135935372
is asnp
is mentioned by
dbSNPrs5929706
ebirs5929706
HLIrs5929706
Exacrs5929706
Varsomers5929706
Maprs5929706
PheGenIrs5929706
hapmaprs5929706
1000 genomesrs5929706
hgdprs5929706
ensemblrs5929706
gopubmedrs5929706
geneviewrs5929706
scholarrs5929706
googlers5929706
pharmgkbrs5929706
gwascentralrs5929706
openSNPrs5929706
23andMers5929706
23andMe allrs5929706
SNP Nexus

SNPshotrs5929706
SNPdbers5929706
MSV3drs5929706
GWAS Ctlgrs5929706
Max Magnitude
? (A;A) (A;C) (C;C) 28

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