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rs7111341

From SNPedia

Orientationplus
Stabilizedplus
Make rs7111341(C;C)
Make rs7111341(C;T)
Make rs7111341(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2191936
is asnp
is mentioned by
dbSNPrs7111341
ebirs7111341
HLIrs7111341
Exacrs7111341
Varsomers7111341
Maprs7111341
PheGenIrs7111341
hapmaprs7111341
1000 genomesrs7111341
hgdprs7111341
ensemblrs7111341
gopubmedrs7111341
geneviewrs7111341
scholarrs7111341
googlers7111341
pharmgkbrs7111341
gwascentralrs7111341
openSNPrs7111341
23andMers7111341
23andMe allrs7111341
SNP Nexus

SNPshotrs7111341
SNPdbers7111341
MSV3drs7111341
GWAS Ctlgrs7111341
GMAF0.253
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19430480OA-icon.png]
Trait Type 1 diabetes
Title Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes
Risk Allele
P-val 4E-48
Odds Ratio NR NR
OMIM125852
Desc
Variant
Relatedalso
OMIM222100
Desc
Variant
Relatedalso
[PMID 19966805OA-icon.png] The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.


GET Evidence
rs7111341
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.28125
summary