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rs2241715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2241715(G;G)
Make rs2241715(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position41350981
GeneTGFB1
is asnp
is mentioned by
dbSNPrs2241715
ebirs2241715
HLIrs2241715
Exacrs2241715
Varsomers2241715
Maprs2241715
PheGenIrs2241715
hapmaprs2241715
1000 genomesrs2241715
hgdprs2241715
ensemblrs2241715
gopubmedrs2241715
geneviewrs2241715
scholarrs2241715
googlers2241715
pharmgkbrs2241715
gwascentralrs2241715
openSNPrs2241715
23andMers2241715
23andMe allrs2241715
SNP Nexus

SNPshotrs2241715
SNPdbers2241715
MSV3drs2241715
GWAS Ctlgrs2241715
GMAF0.3705
Max Magnitude0
? (G;G) (G;T) (T;T) 28
[PMID 19258388OA-icon.png] Genetic variation in the transforming growth factor-{beta}1 gene is associated with susceptibility to IgA nephropathy.


[PMID 19910030OA-icon.png] Evaluation of candidate genes in a genome-wide association study of childhood asthma in Mexicans


[PMID 18292811OA-icon.png] Complex two-gene modulation of lung disease severity in children with cystic fibrosis.


[PMID 20479942OA-icon.png] Genetic risk factors in lupus nephritis and IgA nephropathy--no support of an overlap.


ClinVar
Risk rs2241715(G;G)
Alt rs2241715(G;G)
Reference rs2241715(T;T)
Significance Non-pathogenic
Disease Diaphyseal dysplasia
Variation info
Gene TGFB1
CLNDBN Diaphyseal dysplasia
Reversed 1
HGVS NC_000019.10:g.41350981A>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000032145.1,