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rs7169523

From SNPedia

Orientationplus
Stabilizedplus
Make rs7169523(A;A)
Make rs7169523(A;G)
Make rs7169523(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position31171175
is asnp
is mentioned by
dbSNPrs7169523
ebirs7169523
HLIrs7169523
Exacrs7169523
Varsomers7169523
Maprs7169523
PheGenIrs7169523
hapmaprs7169523
1000 genomesrs7169523
hgdprs7169523
ensemblrs7169523
gopubmedrs7169523
geneviewrs7169523
scholarrs7169523
googlers7169523
pharmgkbrs7169523
gwascentralrs7169523
openSNPrs7169523
23andMers7169523
23andMe allrs7169523
SNP Nexus

SNPshotrs7169523
SNPdbers7169523
MSV3drs7169523
GWAS Ctlgrs7169523
GMAF0.2897
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 2E-6
Odds Ratio 1.40 [1.22-1.60]