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rs16926246

From SNPedia

Orientationplus
Stabilizedplus
Make rs16926246(C;C)
Make rs16926246(C;T)
Make rs16926246(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position69333636
GeneHK1
is asnp
is mentioned by
dbSNPrs16926246
ebirs16926246
HLIrs16926246
Exacrs16926246
Varsomers16926246
Maprs16926246
PheGenIrs16926246
hapmaprs16926246
1000 genomesrs16926246
hgdprs16926246
ensemblrs16926246
gopubmedrs16926246
geneviewrs16926246
scholarrs16926246
googlers16926246
pharmgkbrs16926246
gwascentralrs16926246
openSNPrs16926246
23andMers16926246
23andMe allrs16926246
SNP Nexus

SNPshotrs16926246
SNPdbers16926246
MSV3drs16926246
GWAS Ctlgrs16926246
GMAF0.09963
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Hematocrit
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele T
P-val 1E-13
Odds Ratio 0.33 [0.24-0.42] % increase

[PMID 20858683OA-icon.png] Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways


GET Evidence
rs16926246
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.109375
summary