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rs10495928

From SNPedia

Orientationplus
Stabilizedplus
Make rs10495928(A;A)
Make rs10495928(A;G)
Make rs10495928(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46126027
GenePRKCE
is asnp
is mentioned by
dbSNPrs10495928
ebirs10495928
HLIrs10495928
Exacrs10495928
Varsomers10495928
Maprs10495928
PheGenIrs10495928
hapmaprs10495928
1000 genomesrs10495928
hgdprs10495928
ensemblrs10495928
gopubmedrs10495928
geneviewrs10495928
scholarrs10495928
googlers10495928
pharmgkbrs10495928
gwascentralrs10495928
openSNPrs10495928
23andMers10495928
23andMe allrs10495928
SNP Nexus

SNPshotrs10495928
SNPdbers10495928
MSV3drs10495928
GWAS Ctlgrs10495928
GMAF0.2952
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Hemoglobin
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele G
P-val 7E-13
Odds Ratio 0.06 [0.05-0.08] g/dl increase
GWAS snp
PMID [PMID 20139978]
Trait Hematological and biochemical traits
Title Genome-wide association study of hematological and biochemical traits in a Japanese population
Risk Allele G
P-val 4E-8
Odds Ratio 0.21 [NR] % variance


GET Evidence
rs10495928
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.398438
summary