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rs886424

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs886424(A;A)
Make rs886424(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position30814225
GeneLINC00243
is asnp
is mentioned by
dbSNPrs886424
ebirs886424
HLIrs886424
Exacrs886424
Varsomers886424
Maprs886424
PheGenIrs886424
hapmaprs886424
1000 genomesrs886424
hgdprs886424
ensemblrs886424
gopubmedrs886424
geneviewrs886424
scholarrs886424
googlers886424
pharmgkbrs886424
gwascentralrs886424
openSNPrs886424
23andMers886424
23andMe allrs886424
SNP Nexus

SNPshotrs886424
SNPdbers886424
MSV3drs886424
GWAS Ctlgrs886424
GMAF0.04775
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele
P-val 9E-7
Odds Ratio 1.3700 None


GET Evidence
NCRNA00243-V158M
aa_change Val158Met
aa_change_short V158M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0859375
summary



[PMID 18204098] Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.