rs2286492

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs2286492(G;G)

Make rs2286492(G;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

22945391

Gene

FAM126A

is a	snp
is	mentioned by
dbSNP	rs2286492
dbSNP (classic)	rs2286492
ClinGen	rs2286492
ebi	rs2286492
HLI	rs2286492
Exac	rs2286492
Gnomad	rs2286492
Varsome	rs2286492
LitVar	rs2286492
Map	rs2286492
PheGenI	rs2286492
Biobank	rs2286492
1000 genomes	rs2286492
hgdp	rs2286492
ensembl	rs2286492
geneview	rs2286492
scholar	rs2286492
google	rs2286492
pharmgkb	rs2286492
gwascentral	rs2286492
openSNP	rs2286492
23andMe	rs2286492
SNPshot	rs2286492
SNPdbe	rs2286492
MSV3d	rs2286492
GWAS Ctlg	rs2286492

GMAF

0.07438

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21254220]
Trait
Title	Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.
Risk Allele
P-val	0.000008
Odds Ratio	None None

ClinVar
Risk	rs2286492(G;G)
Alt	rs2286492(G;G)
Reference	Rs2286492(T;T)
Significance	Probable-non-pathogenic
Disease	Hypomyelination and Congenital Cataract
Variation	info
Gene	FAM126A
CLNDBN	Hypomyelination and Congenital Cataract
Reversed	1
HGVS	NC_000007.13:g.22985010A>C
CLNSRC
CLNACC	RCV000281285.1,