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rs11066301

From SNPedia

Orientationplus
Stabilizedplus
Make rs11066301(A;A)
Make rs11066301(A;G)
Make rs11066301(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112433568
GenePTPN11
is asnp
is mentioned by
dbSNPrs11066301
ebirs11066301
HLIrs11066301
Exacrs11066301
Varsomers11066301
Maprs11066301
PheGenIrs11066301
hapmaprs11066301
1000 genomesrs11066301
hgdprs11066301
ensemblrs11066301
gopubmedrs11066301
geneviewrs11066301
scholarrs11066301
googlers11066301
pharmgkbrs11066301
gwascentralrs11066301
openSNPrs11066301
23andMers11066301
23andMe allrs11066301
SNP Nexus

SNPshotrs11066301
SNPdbers11066301
MSV3drs11066301
GWAS Ctlgrs11066301
GMAF0.2006
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait Hematological parameters
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele G
P-val 8E-12
Odds Ratio 4.65 [3.32-5.98] 10^9/l increase


[PMID 19862010OA-icon.png] Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.


[PMID 21193429OA-icon.png] Determinants of platelet count in humans.


GET Evidence
rs11066301
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.195312
summary