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rs7065696

From SNPedia

Orientationplus
Stabilizedplus
Make rs7065696(C;C)
Make rs7065696(C;G)
Make rs7065696(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position53947621
GenePHF8
is asnp
is mentioned by
dbSNPrs7065696
ebirs7065696
HLIrs7065696
Exacrs7065696
Varsomers7065696
Maprs7065696
PheGenIrs7065696
hapmaprs7065696
1000 genomesrs7065696
hgdprs7065696
ensemblrs7065696
gopubmedrs7065696
geneviewrs7065696
scholarrs7065696
googlers7065696
pharmgkbrs7065696
gwascentralrs7065696
openSNPrs7065696
23andMers7065696
23andMe allrs7065696
SNP Nexus

SNPshotrs7065696
SNPdbers7065696
MSV3drs7065696
GWAS Ctlgrs7065696
GMAF0.1215
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 21057379OA-icon.png]
Trait
Title Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes
Risk Allele
P-val 4E-7
Odds Ratio None None