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rs11036238

From SNPedia

Orientationplus
Stabilizedplus
Make rs11036238(C;C)
Make rs11036238(C;G)
Make rs11036238(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position5204405
is asnp
is mentioned by
dbSNPrs11036238
ebirs11036238
HLIrs11036238
Exacrs11036238
Varsomers11036238
Maprs11036238
PheGenIrs11036238
hapmaprs11036238
1000 genomesrs11036238
hgdprs11036238
ensemblrs11036238
gopubmedrs11036238
geneviewrs11036238
scholarrs11036238
googlers11036238
pharmgkbrs11036238
gwascentralrs11036238
openSNPrs11036238
23andMers11036238
23andMe allrs11036238
SNP Nexus

SNPshotrs11036238
SNPdbers11036238
MSV3drs11036238
GWAS Ctlgrs11036238
GMAF0.1488
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19465909OA-icon.png]
Trait Malaria
Title Genome-wide and fine-resolution association anaylsis of malaria in West Africa
Risk Allele
P-val 4E-11
Odds Ratio 1.59 [1.39-1.82]


GET Evidence
rs11036238
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.203125
summary