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rs13021401

From SNPedia

Orientationplus
Stabilizedplus
Make rs13021401(C;C)
Make rs13021401(C;T)
Make rs13021401(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position20488758
is asnp
is mentioned by
dbSNPrs13021401
ebirs13021401
HLIrs13021401
Exacrs13021401
Varsomers13021401
Maprs13021401
PheGenIrs13021401
hapmaprs13021401
1000 genomesrs13021401
hgdprs13021401
ensemblrs13021401
gopubmedrs13021401
geneviewrs13021401
scholarrs13021401
googlers13021401
pharmgkbrs13021401
gwascentralrs13021401
openSNPrs13021401
23andMers13021401
23andMe allrs13021401
SNP Nexus

SNPshotrs13021401
SNPdbers13021401
MSV3drs13021401
GWAS Ctlgrs13021401
GMAF0.3113
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21750679OA-icon.png]
Trait
Title Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.
Risk Allele T
P-val 0.000003
Odds Ratio 1.2100 [1.12-1.31]


[PMID 22896740OA-icon.png] Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study