Have questions? Visit https://www.reddit.com/r/SNPedia

rs7221109

From SNPedia

Orientationplus
Stabilizedplus
Make rs7221109(C;C)
Make rs7221109(C;T)
Make rs7221109(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position40614034
is asnp
is mentioned by
dbSNPrs7221109
ebirs7221109
HLIrs7221109
Exacrs7221109
Varsomers7221109
Maprs7221109
PheGenIrs7221109
hapmaprs7221109
1000 genomesrs7221109
hgdprs7221109
ensemblrs7221109
gopubmedrs7221109
geneviewrs7221109
scholarrs7221109
googlers7221109
pharmgkbrs7221109
gwascentralrs7221109
openSNPrs7221109
23andMers7221109
23andMe allrs7221109
SNP Nexus

SNPshotrs7221109
SNPdbers7221109
MSV3drs7221109
GWAS Ctlgrs7221109
GMAF0.2998
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 1E-9
Odds Ratio 1.05 [0.99-1.12]


GET Evidence
rs7221109
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.734375
summary