Have questions? Visit https://www.reddit.com/r/SNPedia

rs17194885

From SNPedia

Orientationplus
Stabilizedplus
Make rs17194885(A;A)
Make rs17194885(A;C)
Make rs17194885(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position37439987
is asnp
is mentioned by
dbSNPrs17194885
ebirs17194885
HLIrs17194885
Exacrs17194885
Varsomers17194885
Maprs17194885
PheGenIrs17194885
hapmaprs17194885
1000 genomesrs17194885
hgdprs17194885
ensemblrs17194885
gopubmedrs17194885
geneviewrs17194885
scholarrs17194885
googlers17194885
pharmgkbrs17194885
gwascentralrs17194885
openSNPrs17194885
23andMers17194885
23andMe allrs17194885
SNP Nexus

SNPshotrs17194885
SNPdbers17194885
MSV3drs17194885
GWAS Ctlgrs17194885
GMAF0.1198
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 4E-6
Odds Ratio .61 [0.36-0.86] unit decrease