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rs12153855

From SNPedia

Orientationplus
Stabilizedplus
Make rs12153855(C;C)
Make rs12153855(C;T)
Make rs12153855(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32107027
GeneTNXB
is asnp
is mentioned by
dbSNPrs12153855
ebirs12153855
HLIrs12153855
Exacrs12153855
Varsomers12153855
Maprs12153855
PheGenIrs12153855
hapmaprs12153855
1000 genomesrs12153855
hgdprs12153855
ensemblrs12153855
gopubmedrs12153855
geneviewrs12153855
scholarrs12153855
googlers12153855
pharmgkbrs12153855
gwascentralrs12153855
openSNPrs12153855
23andMers12153855
23andMe allrs12153855
SNP Nexus

SNPshotrs12153855
SNPdbers12153855
MSV3drs12153855
GWAS Ctlgrs12153855
GMAF0.1097
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22694956OA-icon.png]
Trait
Title Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.
Risk Allele C
P-val 1E-9
Odds Ratio 1.4400 None
GWAS snp
PMID [PMID 23886662OA-icon.png]
Trait Atopic dermatitis
Title A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.
Risk Allele T
P-val 3E-14
Odds Ratio 1.58 [1.405-1.779]


[PMID 15747258OA-icon.png] A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms.