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rs13153995

From SNPedia

Orientationplus
Stabilizedplus
Make rs13153995(C;C)
Make rs13153995(C;T)
Make rs13153995(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position170197768
GeneLINC01187
is asnp
is mentioned by
dbSNPrs13153995
ebirs13153995
HLIrs13153995
Exacrs13153995
Varsomers13153995
Maprs13153995
PheGenIrs13153995
hapmaprs13153995
1000 genomesrs13153995
hgdprs13153995
ensemblrs13153995
gopubmedrs13153995
geneviewrs13153995
scholarrs13153995
googlers13153995
pharmgkbrs13153995
gwascentralrs13153995
openSNPrs13153995
23andMers13153995
23andMe allrs13153995
SNP Nexus

SNPshotrs13153995
SNPdbers13153995
MSV3drs13153995
GWAS Ctlgrs13153995
Max Magnitude
? (C;C) (C;T) (T;T) 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 3E-6
Odds Ratio 1.22 [1.11-1.33]