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rs5756506

From SNPedia

Orientationplus
Stabilizedplus
Make rs5756506(C;C)
Make rs5756506(C;G)
Make rs5756506(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37071352
GeneTMPRSS6
is asnp
is mentioned by
dbSNPrs5756506
ebirs5756506
HLIrs5756506
Exacrs5756506
Varsomers5756506
Maprs5756506
PheGenIrs5756506
hapmaprs5756506
1000 genomesrs5756506
hgdprs5756506
ensemblrs5756506
gopubmedrs5756506
geneviewrs5756506
scholarrs5756506
googlers5756506
pharmgkbrs5756506
gwascentralrs5756506
openSNPrs5756506
23andMers5756506
23andMe allrs5756506
SNP Nexus

SNPshotrs5756506
SNPdbers5756506
MSV3drs5756506
GWAS Ctlgrs5756506
GMAF0.4757
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 19820697OA-icon.png]
Trait Hematological parameters
Title A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
Risk Allele C
P-val 1E-9
Odds Ratio 0.14 [0.10-0.18] pg increase

[PMID 19673882OA-icon.png] A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.


GET Evidence
rs5756506
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484127
summary