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rs4948088

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A)
(C;C) 0 common on affy axiom data
Make rs4948088(A;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position50959497
is asnp
is mentioned by
dbSNPrs4948088
ClinGenrs4948088
ebirs4948088
HLIrs4948088
Exacrs4948088
Varsomers4948088
Maprs4948088
PheGenIrs4948088
hapmaprs4948088
1000 genomesrs4948088
hgdprs4948088
ensemblrs4948088
gopubmedrs4948088
geneviewrs4948088
scholarrs4948088
googlers4948088
pharmgkbrs4948088
gwascentralrs4948088
openSNPrs4948088
23andMers4948088
23andMe allrs4948088
SNP Nexus

SNPshotrs4948088
SNPdbers4948088
MSV3drs4948088
GWAS Ctlgrs4948088
GMAF0.02525
Max Magnitude0
? (A;A) (A;C) (C;C) 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-8
Odds Ratio 1.30 [1.11-1.49]


GET Evidence
rs4948088
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.965517
summary