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rs4671386

From SNPedia

Orientationplus
Stabilizedplus
Make rs4671386(A;A)
Make rs4671386(A;C)
Make rs4671386(C;C)
ReferenceGRCh38 38.1/142
Chromosome2
Position60287858
is asnp
is mentioned by
dbSNPrs4671386
ebirs4671386
HLIrs4671386
Exacrs4671386
Varsomers4671386
Maprs4671386
PheGenIrs4671386
hapmaprs4671386
1000 genomesrs4671386
hgdprs4671386
ensemblrs4671386
gopubmedrs4671386
geneviewrs4671386
scholarrs4671386
googlers4671386
pharmgkbrs4671386
gwascentralrs4671386
openSNPrs4671386
23andMers4671386
23andMe allrs4671386
SNP Nexus

SNPshotrs4671386
SNPdbers4671386
MSV3drs4671386
GWAS Ctlgrs4671386
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 24927181]
Trait Acne (severe)
Title Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
Risk Allele C
P-val 2E-6
Odds Ratio 1.19 [1.11-1.3]