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rs1399634

From SNPedia

Orientationminus
Stabilizedminus
Make rs1399634(A;A)
Make rs1399634(A;T)
Make rs1399634(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position169388097
is asnp
is mentioned by
dbSNPrs1399634
ebirs1399634
HLIrs1399634
Exacrs1399634
Varsomers1399634
Maprs1399634
PheGenIrs1399634
hapmaprs1399634
1000 genomesrs1399634
hgdprs1399634
ensemblrs1399634
gopubmedrs1399634
geneviewrs1399634
scholarrs1399634
googlers1399634
pharmgkbrs1399634
gwascentralrs1399634
openSNPrs1399634
23andMers1399634
23andMe allrs1399634
SNP Nexus

SNPshotrs1399634
SNPdbers1399634
MSV3drs1399634
GWAS Ctlgrs1399634
GMAF0.4036
Max Magnitude
? (A;A) (A;T) (T;T) 28
[PMID 23562823OA-icon.png] Genome-wide association study in a Chinese population with diabetic retinopathy