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rs1046934

From SNPedia

Orientationplus
Stabilizedplus
Make rs1046934(A;A)
Make rs1046934(A;C)
Make rs1046934(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position184054395
GeneTSEN15
is asnp
is mentioned by
dbSNPrs1046934
ebirs1046934
HLIrs1046934
Exacrs1046934
Varsomers1046934
Maprs1046934
PheGenIrs1046934
hapmaprs1046934
1000 genomesrs1046934
hgdprs1046934
ensemblrs1046934
gopubmedrs1046934
geneviewrs1046934
scholarrs1046934
googlers1046934
pharmgkbrs1046934
gwascentralrs1046934
openSNPrs1046934
23andMers1046934
23andMe allrs1046934
SNP Nexus

SNPshotrs1046934
SNPdbers1046934
MSV3drs1046934
GWAS Ctlgrs1046934
GMAF0.3214
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20881960OA-icon.png]
Trait Height
Title Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele A
P-val 2E-31
Odds Ratio .04 [NR] unit decrease


[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.


[PMID 24944287OA-icon.png] Genetic Variants Related to Height and Risk of Atrial Fibrillation: The Cardiovascular Health Study