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rs1329201

From SNPedia

Orientationminus
Stabilizedminus
Make rs1329201(A;A)
Make rs1329201(A;G)
Make rs1329201(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position81429197
is asnp
is mentioned by
dbSNPrs1329201
ebirs1329201
HLIrs1329201
Exacrs1329201
Varsomers1329201
Maprs1329201
PheGenIrs1329201
hapmaprs1329201
1000 genomesrs1329201
hgdprs1329201
ensemblrs1329201
gopubmedrs1329201
geneviewrs1329201
scholarrs1329201
googlers1329201
pharmgkbrs1329201
gwascentralrs1329201
openSNPrs1329201
23andMers1329201
23andMe allrs1329201
SNP Nexus

SNPshotrs1329201
SNPdbers1329201
MSV3drs1329201
GWAS Ctlgrs1329201
GMAF0.2222
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23393555OA-icon.png]
Trait Retinopathy in non-diabetics
Title Genome-wide association study of retinopathy in individuals without diabetes.
Risk Allele T
P-val 8E-6
Odds Ratio .22 [0.12-0.32] unit decrease