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rs3741208

From SNPedia

Orientationminus
Stabilizedminus
Make rs3741208(C;C)
Make rs3741208(C;T)
Make rs3741208(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2148544
GeneIGF2, INS-IGF2
is asnp
is mentioned by
dbSNPrs3741208
ebirs3741208
HLIrs3741208
Exacrs3741208
Varsomers3741208
Maprs3741208
PheGenIrs3741208
hapmaprs3741208
1000 genomesrs3741208
hgdprs3741208
ensemblrs3741208
gopubmedrs3741208
geneviewrs3741208
scholarrs3741208
googlers3741208
pharmgkbrs3741208
gwascentralrs3741208
openSNPrs3741208
23andMers3741208
23andMe allrs3741208
SNP Nexus

SNPshotrs3741208
SNPdbers3741208
MSV3drs3741208
GWAS Ctlgrs3741208
GMAF0.3421
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 17554260OA-icon.png] associated with type-1 diabetes


[PMID 17980034OA-icon.png] Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'.


[PMID 19639606OA-icon.png] Correcting "winner's curse" in odds ratios from genomewide association findings for major complex human diseases.


[PMID 19956101OA-icon.png] Overview of the Rapid Response data.


[PMID 19956106OA-icon.png] Analysis of 19 genes for association with type I diabetes in the Type I Diabetes Genetics Consortium families.


[PMID 20403199OA-icon.png] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.


GET Evidence
rs3741208
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.578125
summary



Type 1 Diabetes