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

rs6719884

From SNPedia

Orientationplus
Stabilizedplus
Make rs6719884(A;A)
Make rs6719884(A;C)
Make rs6719884(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position58809781
GeneAIRE
is asnp
is mentioned by
dbSNPrs6719884
ebirs6719884
HLIrs6719884
Exacrs6719884
Varsomers6719884
Maprs6719884
PheGenIrs6719884
hapmaprs6719884
1000 genomesrs6719884
hgdprs6719884
ensemblrs6719884
gopubmedrs6719884
geneviewrs6719884
scholarrs6719884
googlers6719884
pharmgkbrs6719884
gwascentralrs6719884
openSNPrs6719884
23andMers6719884
23andMe allrs6719884
SNP Nexus

SNPshotrs6719884
SNPdbers6719884
MSV3drs6719884
GWAS Ctlgrs6719884
GMAF0.449
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23055271OA-icon.png]
Trait Myasthenia gravis
Title Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
Risk Allele A
P-val 3E-6
Odds Ratio 1.35 [1.19-1.52]