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rs1046896

From SNPedia

Orientationplus
Stabilizedplus
Make rs1046896(C;C)
Make rs1046896(C;T)
Make rs1046896(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position82727657
GeneFN3KRP
is asnp
is mentioned by
dbSNPrs1046896
ebirs1046896
HLIrs1046896
Exacrs1046896
Varsomers1046896
Maprs1046896
PheGenIrs1046896
hapmaprs1046896
1000 genomesrs1046896
hgdprs1046896
ensemblrs1046896
gopubmedrs1046896
geneviewrs1046896
scholarrs1046896
googlers1046896
pharmgkbrs1046896
gwascentralrs1046896
openSNPrs1046896
23andMers1046896
23andMe allrs1046896
SNP Nexus

SNPshotrs1046896
SNPdbers1046896
MSV3drs1046896
GWAS Ctlgrs1046896
GMAF0.3861
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 20858683OA-icon.png] Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways
OMIM612940
Desc
Variant
Relatedalso
GWAS snp
PMID [PMID 24244560OA-icon.png]
Trait Glycated hemoglobin levels
Title A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry.
Risk Allele T
P-val 2E-7
Odds Ratio .03 [0.019-0.043] unit increase