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rs497768

From SNPedia

Orientationplus
Stabilizedplus
Make rs497768(C;C)
Make rs497768(C;G)
Make rs497768(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117880025
is asnp
is mentioned by
dbSNPrs497768
ebirs497768
HLIrs497768
Exacrs497768
Varsomers497768
Maprs497768
PheGenIrs497768
hapmaprs497768
1000 genomesrs497768
hgdprs497768
ensemblrs497768
gopubmedrs497768
geneviewrs497768
scholarrs497768
googlers497768
pharmgkbrs497768
gwascentralrs497768
openSNPrs497768
23andMers497768
23andMe allrs497768
SNP Nexus

SNPshotrs497768
SNPdbers497768
MSV3drs497768
GWAS Ctlgrs497768
GMAF0.4247
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 17357072OA-icon.png] associated with schizophrenia rs10790212-rs4938445-rs497768
OMIM603342
DescSCHIZOPHRENIA 2; SCZD2
Variant
Relatedalso
OMIM606683
DescFXYD DOMAIN-CONTAINING ION TRANSPORT REGULATOR 6; FXYD6
Variant
Relatedalso

[PMID 20149392] No association between the FXYD6 gene and schizophrenia in the Chinese Han population.

[PMID 20468077] Failure to confirm genetic association of the FXYD6 gene with schizophrenia: the Japanese population and meta-analysis.