Have questions? Visit https://www.reddit.com/r/SNPedia

rs2075672

From SNPedia

Orientationminus
Stabilizedminus
Make rs2075672(C;C)
Make rs2075672(C;T)
Make rs2075672(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position100642673
GeneACTL6B, TFR2
is asnp
is mentioned by
dbSNPrs2075672
ebirs2075672
HLIrs2075672
Exacrs2075672
Varsomers2075672
Maprs2075672
PheGenIrs2075672
hapmaprs2075672
1000 genomesrs2075672
hgdprs2075672
ensemblrs2075672
gopubmedrs2075672
geneviewrs2075672
scholarrs2075672
googlers2075672
pharmgkbrs2075672
gwascentralrs2075672
openSNPrs2075672
23andMers2075672
23andMe allrs2075672
SNP Nexus

SNPshotrs2075672
SNPdbers2075672
MSV3drs2075672
GWAS Ctlgrs2075672
GMAF0.3186
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 A
P-val 2E-20
Odds Ratio .02 [0.016-0.028] unit increase