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rs6850606

From SNPedia

Orientationplus
Stabilizedplus
Make rs6850606(A;A)
Make rs6850606(A;G)
Make rs6850606(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position42862679
is asnp
is mentioned by
dbSNPrs6850606
ClinGenrs6850606
ebirs6850606
HLIrs6850606
Exacrs6850606
Varsomers6850606
Maprs6850606
PheGenIrs6850606
hapmaprs6850606
1000 genomesrs6850606
hgdprs6850606
ensemblrs6850606
gopubmedrs6850606
geneviewrs6850606
scholarrs6850606
googlers6850606
pharmgkbrs6850606
gwascentralrs6850606
openSNPrs6850606
23andMers6850606
23andMe allrs6850606
SNP Nexus

SNPshotrs6850606
SNPdbers6850606
MSV3drs6850606
GWAS Ctlgrs6850606
GMAF0.421
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 A
P-val 3E-6
Odds Ratio 1.35 [1.19-1.53]