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rs4803455

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs4803455(A;A)
Make rs4803455(A;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position41345604
GeneTGFB1
is asnp
is mentioned by
dbSNPrs4803455
ebirs4803455
HLIrs4803455
Exacrs4803455
Varsomers4803455
Maprs4803455
PheGenIrs4803455
hapmaprs4803455
1000 genomesrs4803455
hgdprs4803455
ensemblrs4803455
gopubmedrs4803455
geneviewrs4803455
scholarrs4803455
googlers4803455
pharmgkbrs4803455
gwascentralrs4803455
openSNPrs4803455
23andMers4803455
23andMe allrs4803455
SNP Nexus

SNPshotrs4803455
SNPdbers4803455
MSV3drs4803455
GWAS Ctlgrs4803455
GMAF0.4784
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 19365037] TGFB1 as a susceptibility gene for high myopia: a replication study with new findings

The T allele appears to be protective against high myopia.


[PMID 21167485] A polymorphism in transforming growth factor-?1 is associated with carotid plaques and increased carotid intima-media thickness in older Chinese men: The Guangzhou Biobank Cohort Study-Cardiovascular Disease Subcohort


[PMID 18424453OA-icon.png] Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis.


[PMID 18670143] The association of transforming growth factor beta 1 gene polymorphisms with the emphysema phenotype of COPD in Japanese.


[PMID 21068203OA-icon.png] Genetic variation in the TGF-beta signaling pathway and colon and rectal cancer risk.


[PMID 23059779] A Study of Ethnic Differences in TGFβ1 Gene Polymorphisms and Effects on the Risk of Radiation Pneumonitis in Non-Small-Cell Lung Cancer


ClinVar
Risk rs4803455(A;A)
Alt rs4803455(A;A)
Reference rs4803455(C;C)
Significance Untested
Disease
Variation info
Gene TGFB1
CLNDBN
Reversed 0
HGVS NC_000019.9:g.41851509C>A
CLNSRC
CLNACC



GWAS snp
PMID [PMID 23793025OA-icon.png]
Trait Migraine
Title Genome-wide meta-analysis identifies new susceptibility loci for migraine.
Risk Allele
P-val 8E-7
Odds Ratio 1.05 [1.03-1.08]