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

rs9977499

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;T) 0 common in complete genomics
Make rs9977499(C;C)
Make rs9977499(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position27362678
is asnp
is mentioned by
dbSNPrs9977499
ebirs9977499
HLIrs9977499
Exacrs9977499
Varsomers9977499
Maprs9977499
PheGenIrs9977499
hapmaprs9977499
1000 genomesrs9977499
hgdprs9977499
ensemblrs9977499
gopubmedrs9977499
geneviewrs9977499
scholarrs9977499
googlers9977499
pharmgkbrs9977499
gwascentralrs9977499
openSNPrs9977499
23andMers9977499
23andMe allrs9977499
SNP Nexus

SNPshotrs9977499
SNPdbers9977499
MSV3drs9977499
GWAS Ctlgrs9977499
GMAF0.3788
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21546767OA-icon.png]
Trait
Title Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes.
Risk Allele
P-val 0.000004
Odds Ratio 1.5700 [1.29-1.91]