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rs6013509

From SNPedia

Orientationplus
Stabilizedplus
Make rs6013509(A;A)
Make rs6013509(A;G)
Make rs6013509(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position52701812
is asnp
is mentioned by
dbSNPrs6013509
ebirs6013509
HLIrs6013509
Exacrs6013509
Varsomers6013509
Maprs6013509
PheGenIrs6013509
hapmaprs6013509
1000 genomesrs6013509
hgdprs6013509
ensemblrs6013509
gopubmedrs6013509
geneviewrs6013509
scholarrs6013509
googlers6013509
pharmgkbrs6013509
gwascentralrs6013509
openSNPrs6013509
23andMers6013509
23andMe allrs6013509
SNP Nexus

SNPshotrs6013509
SNPdbers6013509
MSV3drs6013509
GWAS Ctlgrs6013509
GMAF0.3196
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19862010OA-icon.png]
Trait Hemoglobin
Title Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele A
P-val 1E-10
Odds Ratio 0.06 [0.05-0.08] g/dl decrease


GET Evidence
rs6013509
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.388889
summary