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rs7544736

From SNPedia

Orientationplus
Stabilizedplus
Make rs7544736(A;A)
Make rs7544736(A;G)
Make rs7544736(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position96698787
is asnp
is mentioned by
dbSNPrs7544736
ebirs7544736
HLIrs7544736
Exacrs7544736
Varsomers7544736
Maprs7544736
PheGenIrs7544736
hapmaprs7544736
1000 genomesrs7544736
hgdprs7544736
ensemblrs7544736
gopubmedrs7544736
geneviewrs7544736
scholarrs7544736
googlers7544736
pharmgkbrs7544736
gwascentralrs7544736
openSNPrs7544736
23andMers7544736
23andMe allrs7544736
SNP Nexus

SNPshotrs7544736
SNPdbers7544736
MSV3drs7544736
GWAS Ctlgrs7544736
GMAF0.2296
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19571811OA-icon.png]
Trait Schizophrenia
Title Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Risk Allele G
P-val 6E-7
Odds Ratio 1.25 None


GET Evidence
rs7544736
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary