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rs7552393

From SNPedia

Orientationplus
Stabilizedplus
Make rs7552393(A;A)
Make rs7552393(A;G)
Make rs7552393(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position83788868
GeneRP11-475O6.1
is asnp
is mentioned by
dbSNPrs7552393
ebirs7552393
HLIrs7552393
Exacrs7552393
Varsomers7552393
Maprs7552393
PheGenIrs7552393
hapmaprs7552393
1000 genomesrs7552393
hgdprs7552393
ensemblrs7552393
gopubmedrs7552393
geneviewrs7552393
scholarrs7552393
googlers7552393
pharmgkbrs7552393
gwascentralrs7552393
openSNPrs7552393
23andMers7552393
23andMe allrs7552393
SNP Nexus

SNPshotrs7552393
SNPdbers7552393
MSV3drs7552393
GWAS Ctlgrs7552393
GMAF0.4986
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs7552393
PubMedID [PMID 17903293OA-icon.png]
Condition Select biomarker traits
Gene Intergenic
Risk Allele
pValue 5.00E-007
OR NA
95% CI


[PMID 17903293OA-icon.png] select biomarker trait being TNF-alpha (TNF) levels



GET Evidence
rs7552393
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.460938
summary