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rs1055129

From SNPedia

Orientationminus
Stabilizedminus
Make rs1055129(C;C)
Make rs1055129(C;T)
Make rs1055129(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position75876867
GeneTRIM47
is asnp
is mentioned by
dbSNPrs1055129
ebirs1055129
HLIrs1055129
Exacrs1055129
Varsomers1055129
Maprs1055129
PheGenIrs1055129
hapmaprs1055129
1000 genomesrs1055129
hgdprs1055129
ensemblrs1055129
gopubmedrs1055129
geneviewrs1055129
scholarrs1055129
googlers1055129
pharmgkbrs1055129
gwascentralrs1055129
openSNPrs1055129
23andMers1055129
23andMe allrs1055129
SNP Nexus

SNPshotrs1055129
SNPdbers1055129
MSV3drs1055129
GWAS Ctlgrs1055129
GMAF0.4008
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21681796OA-icon.png]
Trait
Title Genome-wide association studies of cerebral white matter lesion burden: The CHARGE consortium.
Risk Allele G
P-val 3E-11
Odds Ratio None None