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rs7998202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs7998202(A;G)
Make rs7998202(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position112677554
GeneATP11AUN
is asnp
is mentioned by
dbSNPrs7998202
ebirs7998202
HLIrs7998202
Exacrs7998202
Varsomers7998202
Maprs7998202
PheGenIrs7998202
hapmaprs7998202
1000 genomesrs7998202
hgdprs7998202
ensemblrs7998202
gopubmedrs7998202
geneviewrs7998202
scholarrs7998202
googlers7998202
pharmgkbrs7998202
gwascentralrs7998202
openSNPrs7998202
23andMers7998202
23andMe allrs7998202
SNP Nexus

SNPshotrs7998202
SNPdbers7998202
MSV3drs7998202
GWAS Ctlgrs7998202
GMAF0.1543
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20858683OA-icon.png] Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways