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rs7731657

From SNPedia

Orientationplus
Stabilizedplus
Make rs7731657(C;C)
Make rs7731657(C;T)
Make rs7731657(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position130607626
is asnp
is mentioned by
dbSNPrs7731657
dbSNP (old)rs7731657
ClinGenrs7731657
ebirs7731657
HLIrs7731657
Exacrs7731657
Varsomers7731657
Maprs7731657
PheGenIrs7731657
Biobankrs7731657
1000 genomesrs7731657
hgdprs7731657
ensemblrs7731657
gopubmedrs7731657
geneviewrs7731657
scholarrs7731657
googlers7731657
pharmgkbrs7731657
gwascentralrs7731657
openSNPrs7731657
23andMers7731657
23andMe allrs7731657
SNP Nexus

SNPshotrs7731657
SNPdbers7731657
MSV3drs7731657
GWAS Ctlgrs7731657
GMAF0.2897
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903298OA-icon.png]
Trait Fasting plasma glucose
Title Genome-wide association with diabetes-related traits in the Framingham Heart Study
Risk Allele
P-val 0.0000069999999999999999
Odds Ratio NR NR

[PMID 18401594OA-icon.png] Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region.


GET Evidence
rs7731657
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary