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rs56091001

From SNPedia

Orientationplus
Stabilizedplus
Make rs56091001(C;C)
Make rs56091001(C;T)
Make rs56091001(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position49952394
is asnp
is mentioned by
dbSNPrs56091001
ebirs56091001
HLIrs56091001
Exacrs56091001
Varsomers56091001
Maprs56091001
PheGenIrs56091001
hapmaprs56091001
1000 genomesrs56091001
hgdprs56091001
ensemblrs56091001
gopubmedrs56091001
geneviewrs56091001
scholarrs56091001
googlers56091001
pharmgkbrs56091001
gwascentralrs56091001
openSNPrs56091001
23andMers56091001
23andMe allrs56091001
SNP Nexus

SNPshotrs56091001
SNPdbers56091001
MSV3drs56091001
GWAS Ctlgrs56091001
Max Magnitude
GWAS snp
PMID [PMID 24927181]
Trait Acne (severe)
Title Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
Risk Allele T
P-val 4E-6
Odds Ratio 1.28 [1.16-1.42]