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rs10168349

From SNPedia

Orientationplus
Stabilizedplus
Make rs10168349(C;C)
Make rs10168349(C;G)
Make rs10168349(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position46133768
GenePRKCE
is asnp
is mentioned by
dbSNPrs10168349
ebirs10168349
HLIrs10168349
Exacrs10168349
Varsomers10168349
Maprs10168349
PheGenIrs10168349
hapmaprs10168349
1000 genomesrs10168349
hgdprs10168349
ensemblrs10168349
gopubmedrs10168349
geneviewrs10168349
scholarrs10168349
googlers10168349
pharmgkbrs10168349
gwascentralrs10168349
openSNPrs10168349
23andMers10168349
23andMe allrs10168349
SNP Nexus

SNPshotrs10168349
SNPdbers10168349
MSV3drs10168349
GWAS Ctlgrs10168349
GMAF0.2938
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Hematocrit
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele C
P-val 4E-15
Odds Ratio 0.19 [0.14-0.23] % increase


GET Evidence
rs10168349
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.382812
summary



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 5E-7
Odds Ratio .32 [0.193-0.44] unit increase