rs1207463

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs1207463(G;T)

Make rs1207463(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

47811022

is a	snp
is	mentioned by
dbSNP	rs1207463
dbSNP (classic)	rs1207463
ClinGen	rs1207463
ebi	rs1207463
HLI	rs1207463
Exac	rs1207463
Gnomad	rs1207463
Varsome	rs1207463
LitVar	rs1207463
Map	rs1207463
PheGenI	rs1207463
Biobank	rs1207463
1000 genomes	rs1207463
hgdp	rs1207463
ensembl	rs1207463
geneview	rs1207463
scholar	rs1207463
google	rs1207463
pharmgkb	rs1207463
gwascentral	rs1207463
openSNP	rs1207463
23andMe	rs1207463
SNPshot	rs1207463
SNPdbe	rs1207463
MSV3d	rs1207463
GWAS Ctlg	rs1207463

Merged from

Rs17477223

GMAF

0.04716

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

[PMID 23196875] Variants in the 15q25 gene cluster are associated with risk for schizophrenia and bipolar disorder.