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rs9512730

From SNPedia

Orientationplus
Stabilizedplus
Make rs9512730(C;C)
Make rs9512730(C;G)
Make rs9512730(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27503007
is asnp
is mentioned by
dbSNPrs9512730
ebirs9512730
HLIrs9512730
Exacrs9512730
Varsomers9512730
Maprs9512730
PheGenIrs9512730
hapmaprs9512730
1000 genomesrs9512730
hgdprs9512730
ensemblrs9512730
gopubmedrs9512730
geneviewrs9512730
scholarrs9512730
googlers9512730
pharmgkbrs9512730
gwascentralrs9512730
openSNPrs9512730
23andMers9512730
23andMe allrs9512730
SNP Nexus

SNPshotrs9512730
SNPdbers9512730
MSV3drs9512730
GWAS Ctlgrs9512730
GMAF0.2199
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs9512730
PubMedID [PMID 18347602OA-icon.png]
Condition Schizophrenia
Gene Intergenic
Risk Allele
pValue 5.00E-006
OR 1.52
95% CI



[PMID 20823317OA-icon.png] is-rSNP: a novel technique for in silico regulatory SNP detection.


GET Evidence
rs9512730
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary