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rs10510634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10510634(A;G)
Make rs10510634(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position30305477
is asnp
is mentioned by
dbSNPrs10510634
ebirs10510634
HLIrs10510634
Exacrs10510634
Varsomers10510634
Maprs10510634
PheGenIrs10510634
hapmaprs10510634
1000 genomesrs10510634
hgdprs10510634
ensemblrs10510634
gopubmedrs10510634
geneviewrs10510634
scholarrs10510634
googlers10510634
pharmgkbrs10510634
gwascentralrs10510634
openSNPrs10510634
23andMers10510634
23andMe allrs10510634
SNP Nexus

SNPshotrs10510634
SNPdbers10510634
MSV3drs10510634
GWAS Ctlgrs10510634
GMAF0.1455
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs10510634
PubMedID [PMID 17903298OA-icon.png]
Condition Fasting plasma glucose
Gene Intergenic
Risk Allele
pValue 5.00E-006
OR NA
95% CI



GET Evidence
rs10510634
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary