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rs17391694

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs17391694(C;T)
Make rs17391694(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position78157942
is asnp
is mentioned by
dbSNPrs17391694
ebirs17391694
HLIrs17391694
Exacrs17391694
Varsomers17391694
Maprs17391694
PheGenIrs17391694
hapmaprs17391694
1000 genomesrs17391694
hgdprs17391694
ensemblrs17391694
gopubmedrs17391694
geneviewrs17391694
scholarrs17391694
googlers17391694
pharmgkbrs17391694
gwascentralrs17391694
openSNPrs17391694
23andMers17391694
23andMe allrs17391694
SNP Nexus

SNPshotrs17391694
SNPdbers17391694
MSV3drs17391694
GWAS Ctlgrs17391694
GMAF0.04362
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele T
P-val 2E-11
Odds Ratio 0.0400 [NR] meters increase
GWAS snp
PMID [PMID 23128233OA-icon.png]
Trait Crohn's disease
Title Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Risk Allele C
P-val 3E-9
Odds Ratio 1.13 [1.077-1.194]