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rs7529925

From SNPedia

Orientationplus
Stabilizedplus
Make rs7529925(C;C)
Make rs7529925(C;T)
Make rs7529925(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position199038079
is asnp
is mentioned by
dbSNPrs7529925
ebirs7529925
HLIrs7529925
Exacrs7529925
Varsomers7529925
Maprs7529925
PheGenIrs7529925
hapmaprs7529925
1000 genomesrs7529925
hgdprs7529925
ensemblrs7529925
gopubmedrs7529925
geneviewrs7529925
scholarrs7529925
googlers7529925
pharmgkbrs7529925
gwascentralrs7529925
openSNPrs7529925
23andMers7529925
23andMe allrs7529925
SNP Nexus

SNPshotrs7529925
SNPdbers7529925
MSV3drs7529925
GWAS Ctlgrs7529925
GMAF0.2089
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele C
P-val 8E-9
Odds Ratio .01 [0.010-0.018] unit increase