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rs4822752

From SNPedia

Orientationplus
Stabilizedplus
Make rs4822752(C;C)
Make rs4822752(C;T)
Make rs4822752(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position26615456
GeneCRYBB1
is asnp
is mentioned by
dbSNPrs4822752
ebirs4822752
HLIrs4822752
Exacrs4822752
Varsomers4822752
Maprs4822752
PheGenIrs4822752
hapmaprs4822752
1000 genomesrs4822752
hgdprs4822752
ensemblrs4822752
gopubmedrs4822752
geneviewrs4822752
scholarrs4822752
googlers4822752
pharmgkbrs4822752
gwascentralrs4822752
openSNPrs4822752
23andMers4822752
23andMe allrs4822752
SNP Nexus

SNPshotrs4822752
SNPdbers4822752
MSV3drs4822752
GWAS Ctlgrs4822752
GMAF0.3485
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20889312]
Trait Bipolar disorder and schizophrenia
Title A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
Risk Allele
P-val 9E-6
Odds Ratio 1.22 [NR]


[PMID 19503744OA-icon.png] An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.


[PMID 19668596OA-icon.png] A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.