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rs10497721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs10497721(A;A)
Make rs10497721(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position192049636
GeneLOC101927366, TMEFF2
is asnp
is mentioned by
dbSNPrs10497721
ebirs10497721
HLIrs10497721
Exacrs10497721
Varsomers10497721
Maprs10497721
PheGenIrs10497721
hapmaprs10497721
1000 genomesrs10497721
hgdprs10497721
ensemblrs10497721
gopubmedrs10497721
geneviewrs10497721
scholarrs10497721
googlers10497721
pharmgkbrs10497721
gwascentralrs10497721
openSNPrs10497721
23andMers10497721
23andMe allrs10497721
SNP Nexus

SNPshotrs10497721
SNPdbers10497721
MSV3drs10497721
GWAS Ctlgrs10497721
GMAF0.1258
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS
SNP rs10497721
PubMedID [PMID 17903298OA-icon.png]
Condition Incident diabetes
Gene TMEFF2
Risk Allele
pValue 7.00E-007
OR NA
95% CI



GET Evidence
rs10497721
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary