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rs4958881

From SNPedia

Orientationplus
Stabilizedplus
Make rs4958881(C;C)
Make rs4958881(C;T)
Make rs4958881(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position151070675
GeneTNIP1
is asnp
is mentioned by
dbSNPrs4958881
ebirs4958881
HLIrs4958881
Exacrs4958881
Varsomers4958881
Maprs4958881
PheGenIrs4958881
hapmaprs4958881
1000 genomesrs4958881
hgdprs4958881
ensemblrs4958881
gopubmedrs4958881
geneviewrs4958881
scholarrs4958881
googlers4958881
pharmgkbrs4958881
gwascentralrs4958881
openSNPrs4958881
23andMers4958881
23andMe allrs4958881
SNP Nexus

SNPshotrs4958881
SNPdbers4958881
MSV3drs4958881
GWAS Ctlgrs4958881
GMAF0.1938
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22896740OA-icon.png] Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
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 3E-10
Odds Ratio 1.73 [1.46-2.06]