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rs11085824

From SNPedia

Orientationplus
Stabilizedplus
Make rs11085824(A;A)
Make rs11085824(A;G)
Make rs11085824(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position12890733
GeneGCDH
is asnp
is mentioned by
dbSNPrs11085824
ebirs11085824
HLIrs11085824
Exacrs11085824
Varsomers11085824
Maprs11085824
PheGenIrs11085824
hapmaprs11085824
1000 genomesrs11085824
hgdprs11085824
ensemblrs11085824
gopubmedrs11085824
geneviewrs11085824
scholarrs11085824
googlers11085824
pharmgkbrs11085824
gwascentralrs11085824
openSNPrs11085824
23andMers11085824
23andMe allrs11085824
SNP Nexus

SNPshotrs11085824
SNPdbers11085824
MSV3drs11085824
GWAS Ctlgrs11085824
GMAF0.2452
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Mean corpuscular hemoglobin
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele G
P-val 1E-11
Odds Ratio 0 [0.003-0.005] pg decrease


GET Evidence
rs11085824
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.179688
summary