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rs32566

From SNPedia

Orientationplus
Stabilizedplus
Make rs32566(C;C)
Make rs32566(C;T)
Make rs32566(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position5792394
is asnp
is mentioned by
dbSNPrs32566
ebirs32566
HLIrs32566
Exacrs32566
Varsomers32566
Maprs32566
PheGenIrs32566
hapmaprs32566
1000 genomesrs32566
hgdprs32566
ensemblrs32566
gopubmedrs32566
geneviewrs32566
scholarrs32566
googlers32566
pharmgkbrs32566
gwascentralrs32566
openSNPrs32566
23andMers32566
23andMe allrs32566
SNP Nexus

SNPshotrs32566
SNPdbers32566
MSV3drs32566
GWAS Ctlgrs32566
GMAF0.2603
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs32566
PubMedID [PMID 17903295OA-icon.png]
Condition Morbidity-free survival
Gene Intergenic
Risk Allele
pValue 2.00E-009
OR NA
95% CI



GET Evidence
rs32566
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.335938
summary