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rs11642873

From SNPedia

Orientationplus
Stabilizedplus
Make rs11642873(A;A)
Make rs11642873(A;C)
Make rs11642873(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position85958099
is asnp
is mentioned by
dbSNPrs11642873
ebirs11642873
HLIrs11642873
Exacrs11642873
Varsomers11642873
Maprs11642873
PheGenIrs11642873
hapmaprs11642873
1000 genomesrs11642873
hgdprs11642873
ensemblrs11642873
gopubmedrs11642873
geneviewrs11642873
scholarrs11642873
googlers11642873
pharmgkbrs11642873
gwascentralrs11642873
openSNPrs11642873
23andMers11642873
23andMe allrs11642873
SNP Nexus

SNPshotrs11642873
SNPdbers11642873
MSV3drs11642873
GWAS Ctlgrs11642873
GMAF0.1189
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21779181OA-icon.png]
Trait
Title Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
Risk Allele
P-val 2E-12
Odds Ratio 1.3300 [1.23-1.45]