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rs7020996

From SNPedia

Orientationplus
Stabilizedplus
Make rs7020996(C;C)
Make rs7020996(C;T)
Make rs7020996(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22129580
is asnp
is mentioned by
dbSNPrs7020996
ebirs7020996
HLIrs7020996
Exacrs7020996
Varsomers7020996
Maprs7020996
PheGenIrs7020996
hapmaprs7020996
1000 genomesrs7020996
hgdprs7020996
ensemblrs7020996
gopubmedrs7020996
geneviewrs7020996
scholarrs7020996
googlers7020996
pharmgkbrs7020996
gwascentralrs7020996
openSNPrs7020996
23andMers7020996
23andMe allrs7020996
SNP Nexus

SNPshotrs7020996
SNPdbers7020996
MSV3drs7020996
GWAS Ctlgrs7020996
GMAF0.2484
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18372903OA-icon.png]
Trait Type 2 diabetes
Title Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
Risk Allele C
P-val 1.9999999999999999E-7
Odds Ratio 1.26 [1.15-1.38]


[PMID 20580033] Replication of recently described type 2 diabetes gene variants in a South Indian population.


GET Evidence
rs7020996
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.1875
summary