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rs146692665

From SNPedia

Orientationplus
Stabilizedplus
Make rs146692665(G;G)
Make rs146692665(G;T)
Make rs146692665(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position45343191
GeneLOC105377062
is asnp
is mentioned by
dbSNPrs146692665
dbSNP (old)rs146692665
ClinGenrs146692665
ebirs146692665
HLIrs146692665
Exacrs146692665
Gnomadrs146692665
Varsomers146692665
Maprs146692665
PheGenIrs146692665
Biobankrs146692665
1000 genomesrs146692665
hgdprs146692665
ensemblrs146692665
gopubmedrs146692665
geneviewrs146692665
scholarrs146692665
googlers146692665
pharmgkbrs146692665
gwascentralrs146692665
openSNPrs146692665
23andMers146692665
23andMe allrs146692665
SNP Nexus

SNPshotrs146692665
SNPdbers146692665
MSV3drs146692665
GWAS Ctlgrs146692665
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 3E-6
Odds Ratio 2.17 [1.45-3.24]