rs497768

Orientation

plus

Stabilized

plus

Make rs497768(C;C)

Make rs497768(C;G)

Make rs497768(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

117880025

is a	snp
is	mentioned by
dbSNP	rs497768
dbSNP (classic)	rs497768
ClinGen	rs497768
ebi	rs497768
HLI	rs497768
Exac	rs497768
Gnomad	rs497768
Varsome	rs497768
LitVar	rs497768
Map	rs497768
PheGenI	rs497768
Biobank	rs497768
1000 genomes	rs497768
hgdp	rs497768
ensembl	rs497768
geneview	rs497768
scholar	rs497768
google	rs497768
pharmgkb	rs497768
gwascentral	rs497768
openSNP	rs497768
23andMe	rs497768
SNPshot	rs497768
SNPdbe	rs497768
MSV3d	rs497768
GWAS Ctlg	rs497768

GMAF

0.4247

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 17357072] associated with schizophrenia rs10790212-rs4938445-rs497768

OMIM	603342
Desc	SCHIZOPHRENIA 2; SCZD2
Variant
Related	also

OMIM	606683
Desc	FXYD DOMAIN-CONTAINING ION TRANSPORT REGULATOR 6; FXYD6
Variant
Related	also

[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.