Have questions? Visit https://www.reddit.com/r/SNPedia

rs11970772

From SNPedia

Orientationplus
Stabilizedplus
Make rs11970772(A;A)
Make rs11970772(A;T)
Make rs11970772(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position41957552
GeneCCND3
is asnp
is mentioned by
dbSNPrs11970772
ebirs11970772
HLIrs11970772
Exacrs11970772
Varsomers11970772
Maprs11970772
PheGenIrs11970772
hapmaprs11970772
1000 genomesrs11970772
hgdprs11970772
ensemblrs11970772
gopubmedrs11970772
geneviewrs11970772
scholarrs11970772
googlers11970772
pharmgkbrs11970772
gwascentralrs11970772
openSNPrs11970772
23andMers11970772
23andMe allrs11970772
SNP Nexus

SNPshotrs11970772
SNPdbers11970772
MSV3drs11970772
GWAS Ctlgrs11970772
GMAF0.315
Max Magnitude
? (A;A) (A;T) (T;T) 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 T
P-val 7E-19
Odds Ratio 0.58 [0.44-0.70] fl increase


GET Evidence
rs11970772
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.273438
summary