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rs746961

From SNPedia

Orientationminus
Stabilizedminus
Make rs746961(C;C)
Make rs746961(C;T)
Make rs746961(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position30608983
GeneZNF536
is asnp
is mentioned by
dbSNPrs746961
ebirs746961
HLIrs746961
Exacrs746961
Varsomers746961
Maprs746961
PheGenIrs746961
hapmaprs746961
1000 genomesrs746961
hgdprs746961
ensemblrs746961
gopubmedrs746961
geneviewrs746961
scholarrs746961
googlers746961
pharmgkbrs746961
gwascentralrs746961
openSNPrs746961
23andMers746961
23andMe allrs746961
SNP Nexus

SNPshotrs746961
SNPdbers746961
MSV3drs746961
GWAS Ctlgrs746961
GMAF0.4789
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs746961
PubMedID [PMID 17903293OA-icon.png]
Condition Select biomarker traits
Gene ZNF536
Risk Allele
pValue 8.00E-007
OR NA
95% CI



GET Evidence
rs746961
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency
summary