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rs416603

From SNPedia

Orientationplus
Stabilizedplus
Make rs416603(A;A)
Make rs416603(A;T)
Make rs416603(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position11270222
GeneTNP2
is asnp
is mentioned by
dbSNPrs416603
ebirs416603
HLIrs416603
Exacrs416603
Varsomers416603
Maprs416603
PheGenIrs416603
hapmaprs416603
1000 genomesrs416603
hgdprs416603
ensemblrs416603
gopubmedrs416603
geneviewrs416603
scholarrs416603
googlers416603
pharmgkbrs416603
gwascentralrs416603
openSNPrs416603
23andMers416603
23andMe allrs416603
SNP Nexus

SNPshotrs416603
SNPdbers416603
MSV3drs416603
GWAS Ctlgrs416603
GMAF0.3815
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 18978792OA-icon.png]
Trait Type 1 diabetes
Title Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci
Risk Allele T
P-val 0.0000030000000000000001
Odds Ratio 1.06 [1.01-1.12]



GET Evidence
rs416603
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484375
summary