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rs10758658

From SNPedia

Orientationplus
Stabilizedplus
Make rs10758658(A;A)
Make rs10758658(A;G)
Make rs10758658(G;G)
ReferenceGRCh37 37.1/131
Chromosome9
Position4856877
GeneRCL1
is asnp
is mentioned by
dbSNPrs10758658
ebirs10758658
HLIrs10758658
Exacrs10758658
Varsomers10758658
Maprs10758658
PheGenIrs10758658
hapmaprs10758658
1000 genomesrs10758658
hgdprs10758658
ensemblrs10758658
gopubmedrs10758658
geneviewrs10758658
scholarrs10758658
googlers10758658
pharmgkbrs10758658
gwascentralrs10758658
openSNPrs10758658
23andMers10758658
23andMe allrs10758658
SNP Nexus

SNPshotrs10758658
SNPdbers10758658
MSV3drs10758658
GWAS Ctlgrs10758658
GMAF0.225
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 A
P-val 2E-14
Odds Ratio 0 [0.004-0.006] pg decrease


GET Evidence
rs10758658
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.171875
summary